JPS60252430A - アセチレン化合物類の製法 - Google Patents

アセチレン化合物類の製法

Info

Publication number: JPS60252430A
Authority: JP; Japan
Prior art keywords: group; tert; formula; compound; positive integer
Prior art date: 1984-05-29
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Granted

Application number

JP59110230A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0355452B2 (fi

Inventor

Junzo Odera

純蔵大寺

Tadakatsu Bandai

忠勝萬代

Mikio Kawada

河田　幹夫

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Osaka Soda Co Ltd

Original Assignee

Osaka Soda Co Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1984-05-29

Filing date

1984-05-29

Publication date

1985-12-13

1984-05-29 Application filed by Osaka Soda Co Ltd filed Critical Osaka Soda Co Ltd

1984-05-29 Priority to JP59110230A priority Critical patent/JPS60252430A/ja

1985-12-13 Publication of JPS60252430A publication Critical patent/JPS60252430A/ja

1991-08-23 Publication of JPH0355452B2 publication Critical patent/JPH0355452B2/ja

Status Granted legal-status Critical Current

Links

238000004519 manufacturing process Methods 0.000 title claims description 5
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 title description 2
-1 acetylene compound Chemical class 0.000 title 1
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 8
LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 claims abstract description 8
150000003457 sulfones Chemical class 0.000 claims abstract description 8
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims abstract description 8
239000004215 Carbon black (E152) Substances 0.000 claims abstract description 3
125000003118 aryl group Chemical group 0.000 claims abstract description 3
229930195733 hydrocarbon Natural products 0.000 claims abstract description 3
150000002430 hydrocarbons Chemical group 0.000 claims abstract description 3
125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 3
125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 7
238000006243 chemical reaction Methods 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
125000006239 protecting group Chemical group 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
230000002411 adverse Effects 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
150000001875 compounds Chemical class 0.000 abstract description 8
230000006326 desulfonation Effects 0.000 abstract description 2
238000005869 desulfonation reaction Methods 0.000 abstract description 2
238000005906 dihydroxylation reaction Methods 0.000 abstract description 2
239000000203 mixture Substances 0.000 abstract 1
239000000126 substance Substances 0.000 abstract 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 4
239000007858 starting material Substances 0.000 description 4
239000011203 carbon fibre reinforced carbon Substances 0.000 description 3
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
238000000034 method Methods 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
239000007806 chemical reaction intermediate Substances 0.000 description 1
239000007810 chemical reaction solvent Substances 0.000 description 1
238000011097 chromatography purification Methods 0.000 description 1
150000002440 hydroxy compounds Chemical class 0.000 description 1
150000002641 lithium Chemical class 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000012046 mixed solvent Substances 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
235000021419 vinegar Nutrition 0.000 description 1
239000000052 vinegar Substances 0.000 description 1

Classifications

- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

Furan Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP59110230A 1984-05-29 1984-05-29 アセチレン化合物類の製法 Granted JPS60252430A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP59110230A JPS60252430A (ja)	1984-05-29	1984-05-29	アセチレン化合物類の製法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP59110230A JPS60252430A (ja)	1984-05-29	1984-05-29	アセチレン化合物類の製法

Publications (2)

Publication Number	Publication Date
JPS60252430A true JPS60252430A (ja)	1985-12-13
JPH0355452B2 JPH0355452B2 (fi)	1991-08-23

Family

ID=14530390

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP59110230A Granted JPS60252430A (ja)	1984-05-29	1984-05-29	アセチレン化合物類の製法

Country Status (1)

Country	Link
JP (1)	JPS60252430A (fi)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2011173830A (ja) *	2010-02-24	2011-09-08	Nippon Zeon Co Ltd	アルキンの製造方法及び２−ブチンの精製方法

1984
- 1984-05-29 JP JP59110230A patent/JPS60252430A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2011173830A (ja) *	2010-02-24	2011-09-08	Nippon Zeon Co Ltd	アルキンの製造方法及び２−ブチンの精製方法

Also Published As

Publication number	Publication date
JPH0355452B2 (fi)	1991-08-23

Publication	Publication Date	Title
JPH05506446A (ja)	1993-09-22	フェニルイソセリン誘導体類のエナンチオ選択的製造方法
JPS6140668B2 (fi)	1986-09-10
WO1986002923A1 (en)	1986-05-22	Process for preparing bicyclo ad3.3.0 bdoctenes
JPS60252430A (ja)	1985-12-13	アセチレン化合物類の製法
JPH05286894A (ja)	1993-11-02	カルボン酸エステル又はカルボン酸チオエステルの新規製造方法
JPS60252431A (ja)	1985-12-13	共役不飽和化合物の製法
SU371245A1 (ru)	1973-02-22	Способ получения дипропаргилового эфира 1-окси-2, 2, 2-трихлорэтилфосфоновой кислоты
JPH0466219B2 (fi)	1992-10-22
JP2579547B2 (ja)	1997-02-05	アルコキシカルボニル化合物の製法
JPS61145139A (ja)	1986-07-02	コレカルシフエロール誘導体
KR940006531B1 (ko)	1994-07-21	피리딘 유도체의 제조방법
JPS61155352A (ja)	1986-07-15	４−クロロ−３−アルケン酸およびその製造方法
JP3474009B2 (ja)	2003-12-08	チーグラーナッタ触媒の電子供与性化合物として有効なエステル化合物の製造方法
KR100935016B1 (ko)	2010-01-06	1-(2-하이드록시페닐)부타-2-엔-1-온 또는 크로만-4-온 유도체의 제조방법
JPH047349B2 (fi)	1992-02-10
JPH0325421B2 (fi)	1991-04-05
JP2652248B2 (ja)	1997-09-10	アルコキシニトリル化合物の製法
JPS6332358B2 (fi)	1988-06-29
JPH0415233B2 (fi)	1992-03-17
JPH07138282A (ja)	1995-05-30	２４―オキソコレステロール類の製造法
JPS60190744A (ja)	1985-09-28	アミノ酸誘導体の製造法
JPS6024796B2 (ja)	1985-06-14	ボラン錯化合物及びその製造法
JPH0370717B2 (fi)	1991-11-08
JPS60169433A (ja)	1985-09-02	アセチレニツクケトン類の製造法
JPS5978196A (ja)	1984-05-04	ｓｙｍ−ジメチルジ−ｔｅｒｔ−ブチルジクロロジシラン

Legal Events

Date	Code	Title	Description
2003-08-23	LAPS	Cancellation because of no payment of annual fees

JPS60252430A - アセチレン化合物類の製法 - Google Patents

Info

Links

Classifications

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=14530390

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

Also Published As

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Legal Events