GB1132034A - Brominating butyne-(2)-diol-(1,4) - Google Patents
Brominating butyne-(2)-diol-(1,4)Info
- Publication number
- GB1132034A GB1132034A GB8107/66A GB810766A GB1132034A GB 1132034 A GB1132034 A GB 1132034A GB 8107/66 A GB8107/66 A GB 8107/66A GB 810766 A GB810766 A GB 810766A GB 1132034 A GB1132034 A GB 1132034A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diol
- bromination
- butyne
- brominating
- tetrabromotetrahydrofuran
- Prior art date
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/62—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/20—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/05—Alcohols; Metal alcoholates
- C08K5/053—Polyhydroxylic alcohols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
1,132,034. Bromination of butyne-(2)-diol- (1,4). BADISCHE ANILIN- & SODAFABRIK A.G. 24 Feb., 1966 [25 Feb., 1965], No. 8107/66. Heading C2C. [Also in Division C3] The invention comprises 2,2,3,3-tetrabromobutanediol-(1,4 and 2-hydroxy-3,3,4,4-tetrabromotetrahydrofuran and a general process for brominating butyne-(2)-diol-(1,4) to give a reaction product including at least one of 2,2,3,3 - tetrabromobutanediol - (1,4), 2,3 - dibromobutene - (2) - diol - (1,4), 2 - hydroxy - 3,3,4,4 - tetrabromotetrahydrofuran and mucobromic acid, by contacting the diol with bromine in an aqueous or aqueous mineral acid medium at - 40‹ to 140‹ C. The bromination may be effected using U.V. radiation or known halogenation catalysts. Suitable adjustment of the reaction conditions can direct the bromination to give only one or two of the above products. The bromination products may be used to impart a flame-resistant finish to plastics (see Division C3). Examples are provided.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB80711A DE1277244B (en) | 1965-02-25 | 1965-02-25 | Process for the preparation of 2,3-dibromobutene- (2) -diol- (1,4), 2,2,3,3-tetrabromobutanediol- (1,4) and / or mucobromic acid |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1132034A true GB1132034A (en) | 1968-10-30 |
Family
ID=6980821
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8107/66A Expired GB1132034A (en) | 1965-02-25 | 1966-02-24 | Brominating butyne-(2)-diol-(1,4) |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE676870A (en) |
DE (1) | DE1277244B (en) |
GB (1) | GB1132034A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3681468A (en) * | 1970-03-17 | 1972-08-01 | Great Lakes Chemical Corp | Process for the production of halogenated alcohols |
US3764546A (en) * | 1971-03-10 | 1973-10-09 | Ici America Inc | Alkoxylated dihalobutenediol containing compositions |
US4431852A (en) * | 1981-05-12 | 1984-02-14 | Imperial Chemical Industries Limited | Halohydrins |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1303047C (en) * | 2004-03-29 | 2007-03-07 | 上海三爱思试剂有限公司 | Method for preparing 2,3-dibromo-2-butene-1,4-glycol |
-
1965
- 1965-02-25 DE DEB80711A patent/DE1277244B/en active Pending
-
1966
- 1966-02-22 BE BE676870D patent/BE676870A/xx unknown
- 1966-02-24 GB GB8107/66A patent/GB1132034A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3681468A (en) * | 1970-03-17 | 1972-08-01 | Great Lakes Chemical Corp | Process for the production of halogenated alcohols |
US3764546A (en) * | 1971-03-10 | 1973-10-09 | Ici America Inc | Alkoxylated dihalobutenediol containing compositions |
US4431852A (en) * | 1981-05-12 | 1984-02-14 | Imperial Chemical Industries Limited | Halohydrins |
Also Published As
Publication number | Publication date |
---|---|
BE676870A (en) | 1966-08-22 |
DE1277244B (en) | 1968-09-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1132083A (en) | A novel thymine derivative and a process for the preparation thereof | |
GB1411524A (en) | Process for the preparation of brominated aromatic compounds | |
GB1333489A (en) | Process for preparing beta, beta,-bis-3,5-dibromo-4-hydroxy phenyl-propane | |
GB1377550A (en) | Quinazarin derivative | |
GB1132034A (en) | Brominating butyne-(2)-diol-(1,4) | |
GB1016016A (en) | Process for the manufacture of hexafluoropropene | |
GB1145778A (en) | Process for isolating acrylic acid from the reaction gases obtained by the oxidationof propylene or acrolein | |
GB1250505A (en) | ||
GB1316415A (en) | Process for the preparation of tetrabromo bisphenol | |
GB1329815A (en) | Production of tertiary acetylenic glycols by reaction of acetylene with ketones | |
GB1252533A (en) | ||
GB1167645A (en) | Production of Acetals of Methylglyoxal | |
GB1311115A (en) | Process for the manufacture of para-tertiary butylphenol | |
GB1276911A (en) | New basic mono-azo dyes of the indazole series | |
GB1074842A (en) | Improvements in projection system | |
GB1333845A (en) | 1-phenyl-4-acetoacetamino-5-halopyridazones-6 | |
GB1298480A (en) | Process for the production of diaminodiphenyl methanes | |
GB1190228A (en) | 5-Chloro-2,3-Pyridine Diol and a Process for its Production | |
GB1149447A (en) | A process for the preparation of orcinol | |
ITO | Scientifical Control at Hitachi Mill | |
GB1191509A (en) | Production of beta-Chloroalkyl Sulfochlorides and beta-Bromoalkyl Sulfobromides. | |
GB1143930A (en) | Process for the preparation of an acid fluoride and of corresponding esters | |
GB1227245A (en) | ||
GB1316357A (en) | Mono-ortho-alkylation of p-alkoxyphenols | |
GB1274889A (en) | Pure 2,3,6-trimethylphenol |