ZA846600B - Process for the manufacture of trans-1.1.2.3.4.4-hexabromo-2-butene(hbb)by the bromination of diacetylene - Google Patents

Process for the manufacture of trans-1.1.2.3.4.4-hexabromo-2-butene(hbb)by the bromination of diacetylene

Info

Publication number
ZA846600B
ZA846600B ZA846600A ZA846600A ZA846600B ZA 846600 B ZA846600 B ZA 846600B ZA 846600 A ZA846600 A ZA 846600A ZA 846600 A ZA846600 A ZA 846600A ZA 846600 B ZA846600 B ZA 846600B
Authority
ZA
South Africa
Prior art keywords
diacetylene
degrees
bar
temperature
pressure
Prior art date
Application number
ZA846600A
Inventor
Reinhold Zillmann
Original Assignee
Huels Chemische Werke Ag
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.)
Filing date
Publication date
Application filed by Huels Chemische Werke Ag filed Critical Huels Chemische Werke Ag
Publication of ZA846600B publication Critical patent/ZA846600B/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/013Preparation of halogenated hydrocarbons by addition of halogens
    • C07C17/02Preparation of halogenated hydrocarbons by addition of halogens to unsaturated hydrocarbons

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Physical Deposition Of Substances That Are Components Of Semiconductor Devices (AREA)

Abstract

1. A process for the production of trans 1,1,2,3,4,4-hexabromo-2-butene by bromination of diacetylene, characterised in that the diacetylene from the hydrocarbon residue arising in the acetylene recovery operation is dissolved at a temperature of -20 degrees C to + 20 degrees C and a pressure of 1 to 2 bar in a solvent containing a hydroxyl group, initially a mixture rich in vinylacetylene is separated off in a first desorption stage at a temperature of 0 to 30 degrees C and a pressure of 1 to 2 bar with an inert gas, then a gas mixture rich in diacetylene is desorbed in a second desorption stage at a temperature of 0 to 30 degrees C and a pressure of 1 to 2 bar with an inert gas, this diacetylene-rich gas mixture is brominated in a reactor in which excess bromine dissolved in a halohydrocarbon has previously been placed, water optionally being added to the halohydrocarbon, at a temperature of 20 to 40 degrees C and a pressure of 1.2 to 2 bar to form trans 1,1,2,3,4,4- hexabromo-2-butene, gaseous bromine being additionally fed to the reactor with the reaction gas, and the bromine-containing offgas is optionally reacted in an after-reactor with excess diacetylene in a halohydrocarbon.
ZA846600A 1983-08-25 1984-08-24 Process for the manufacture of trans-1.1.2.3.4.4-hexabromo-2-butene(hbb)by the bromination of diacetylene ZA846600B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE3330608A DE3330608A1 (en) 1983-08-25 1983-08-25 METHOD FOR PRODUCING TRANS-1.1.2.3.4.4-HEXABROM-2-BUTEN (HBB) BY BRROMING DIACETYLENE

Publications (1)

Publication Number Publication Date
ZA846600B true ZA846600B (en) 1985-04-24

Family

ID=6207376

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA846600A ZA846600B (en) 1983-08-25 1984-08-24 Process for the manufacture of trans-1.1.2.3.4.4-hexabromo-2-butene(hbb)by the bromination of diacetylene

Country Status (9)

Country Link
EP (1) EP0133911B1 (en)
JP (1) JPS6089438A (en)
AT (1) ATE27448T1 (en)
CA (1) CA1229626A (en)
DE (2) DE3330608A1 (en)
NO (1) NO157016C (en)
RO (1) RO89861A2 (en)
SU (1) SU1225478A3 (en)
ZA (1) ZA846600B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4885233B2 (en) * 2005-11-10 2012-02-29 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Composition, anti-combustion composition, anti-combustion and / or extinguishing method, anti-combustion system and production method

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1360050A (en) * 1970-11-20 1974-07-17 Tenneco Chem Polyhalogenated aliphatic hydrocarbons
US4107230A (en) * 1974-05-08 1978-08-15 Tenneco Chemicals, Inc. Flame-retardant thermosetting resinous compositions

Also Published As

Publication number Publication date
CA1229626A (en) 1987-11-24
DE3463927D1 (en) 1987-07-02
NO157016B (en) 1987-09-28
EP0133911A2 (en) 1985-03-13
ATE27448T1 (en) 1987-06-15
JPS6089438A (en) 1985-05-20
EP0133911B1 (en) 1987-05-27
EP0133911A3 (en) 1986-02-12
NO157016C (en) 1988-01-06
SU1225478A3 (en) 1986-04-15
RO89861A2 (en) 1986-09-30
NO843350L (en) 1985-02-26
DE3330608A1 (en) 1985-03-07

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