NL137306C - - Google Patents
Info
- Publication number
- NL137306C NL137306C NL137306DA NL137306C NL 137306 C NL137306 C NL 137306C NL 137306D A NL137306D A NL 137306DA NL 137306 C NL137306 C NL 137306C
- Authority
- NL
- Netherlands
- Prior art keywords
- nitro
- chloro
- substituent
- group
- chloride
- Prior art date
Links
- 125000001424 substituent group Chemical group 0.000 abstract 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 5
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 5
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 5
- 239000003085 diluting agent Substances 0.000 abstract 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 3
- 239000000460 chlorine Substances 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 150000002828 nitro derivatives Chemical class 0.000 abstract 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- LRVYWUBCXYZLBH-UHFFFAOYSA-N 1,3-dinitronaphthalene-2-carbonitrile Chemical compound [N+](=O)([O-])C1=C(C(=CC2=CC=CC=C12)[N+](=O)[O-])C#N LRVYWUBCXYZLBH-UHFFFAOYSA-N 0.000 abstract 1
- JSBDLOYGWAITKA-UHFFFAOYSA-N 1-chloro-2-(chloromethyl)-3-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC(Cl)=C1CCl JSBDLOYGWAITKA-UHFFFAOYSA-N 0.000 abstract 1
- DGXGEZKTQKVDSV-UHFFFAOYSA-N 1-chloro-2-(dichloromethyl)-3-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC(Cl)=C1C(Cl)Cl DGXGEZKTQKVDSV-UHFFFAOYSA-N 0.000 abstract 1
- YOYAIZYFCNQIRF-UHFFFAOYSA-N 2,6-dichlorobenzonitrile Chemical compound ClC1=CC=CC(Cl)=C1C#N YOYAIZYFCNQIRF-UHFFFAOYSA-N 0.000 abstract 1
- ZYDGHQSJZAFMLU-UHFFFAOYSA-N 2,6-dinitrobenzonitrile Chemical compound [O-][N+](=O)C1=CC=CC([N+]([O-])=O)=C1C#N ZYDGHQSJZAFMLU-UHFFFAOYSA-N 0.000 abstract 1
- ZHLCARBDIRRRHD-UHFFFAOYSA-N 2-chloro-6-nitrobenzonitrile Chemical compound [O-][N+](=O)C1=CC=CC(Cl)=C1C#N ZHLCARBDIRRRHD-UHFFFAOYSA-N 0.000 abstract 1
- XCSNRORTQRKCHB-UHFFFAOYSA-N 2-chloro-6-nitrotoluene Chemical compound CC1=C(Cl)C=CC=C1[N+]([O-])=O XCSNRORTQRKCHB-UHFFFAOYSA-N 0.000 abstract 1
- SWBDKCMOLSUXRH-UHFFFAOYSA-N 2-nitrobenzonitrile Chemical compound [O-][N+](=O)C1=CC=CC=C1C#N SWBDKCMOLSUXRH-UHFFFAOYSA-N 0.000 abstract 1
- PLAZTCDQAHEYBI-UHFFFAOYSA-N 2-nitrotoluene Chemical compound CC1=CC=CC=C1[N+]([O-])=O PLAZTCDQAHEYBI-UHFFFAOYSA-N 0.000 abstract 1
- DAFDUOSMRRTLRZ-UHFFFAOYSA-N 3-chloro-1-nitronaphthalene-2-carbonitrile Chemical compound ClC=1C(=C(C2=CC=CC=C2C1)[N+](=O)[O-])C#N DAFDUOSMRRTLRZ-UHFFFAOYSA-N 0.000 abstract 1
- MGWGWNFMUOTEHG-UHFFFAOYSA-N 4-(3,5-dimethylphenyl)-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CC(C=2N=C(N)SC=2)=C1 MGWGWNFMUOTEHG-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 1
- 239000004157 Nitrosyl chloride Substances 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 150000001491 aromatic compounds Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
- 239000007792 gaseous phase Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- -1 hydrocarbon radical Chemical class 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- 239000007791 liquid phase Substances 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- VPCDQGACGWYTMC-UHFFFAOYSA-N nitrosyl chloride Chemical compound ClN=O VPCDQGACGWYTMC-UHFFFAOYSA-N 0.000 abstract 1
- 235000019392 nitrosyl chloride Nutrition 0.000 abstract 1
- 239000007800 oxidant agent Substances 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 150000002978 peroxides Chemical class 0.000 abstract 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B39/00—Halogenation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL283614 | 1962-09-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL137306C true NL137306C (de) |
Family
ID=19754134
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL283614D NL283614A (de) | 1962-09-25 | ||
| NL137306D NL137306C (de) | 1962-09-25 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL283614D NL283614A (de) | 1962-09-25 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3265603A (de) |
| BE (1) | BE637746A (de) |
| CH (1) | CH454815A (de) |
| DE (1) | DE1267206B (de) |
| DK (1) | DK119702B (de) |
| GB (1) | GB987000A (de) |
| NL (2) | NL137306C (de) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2920173A1 (de) * | 1979-05-18 | 1980-12-04 | Hoechst Ag | Verfahren zur herstellung von 1,3,5-trichlorbenzol |
| DE19937025A1 (de) * | 1999-08-05 | 2001-02-15 | Bayer Ag | Verfahren zur Herstellung von gegebenenfalls substituierten Dichloraromaten |
| KR20210092214A (ko) | 2018-11-16 | 2021-07-23 | 아리스타 라이프사이언스 인코포레이티드 | 2,6-다이클로로벤조니트릴의 제조 공정 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2010841A (en) * | 1933-07-21 | 1935-08-13 | Great Western Electro Chemical Co | Chlorination |
| US2459423A (en) * | 1942-04-08 | 1949-01-18 | Colgate Palmolive Peet Co | Reaction of organic compounds with hydrogen halides |
| US2429031A (en) * | 1945-02-23 | 1947-10-14 | Wingfoot Corp | Halogenation of alpha, beta-unsaturated nitriles |
-
0
- NL NL283614D patent/NL283614A/xx unknown
- NL NL137306D patent/NL137306C/xx active
- BE BE637746D patent/BE637746A/xx unknown
-
1963
- 1963-09-06 US US307035A patent/US3265603A/en not_active Expired - Lifetime
- 1963-09-23 GB GB37376/63A patent/GB987000A/en not_active Expired
- 1963-09-23 DE DEP1267A patent/DE1267206B/de active Pending
- 1963-09-23 CH CH1170263A patent/CH454815A/de unknown
- 1963-09-24 DK DK449363AA patent/DK119702B/da unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US3265603A (en) | 1966-08-09 |
| DK119702B (da) | 1971-02-15 |
| CH454815A (de) | 1968-04-30 |
| NL283614A (de) | |
| GB987000A (en) | 1965-03-24 |
| BE637746A (de) | |
| DE1267206B (de) | 1968-05-02 |
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| NL137306C (de) | ||
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