GB925467A - Production of pentaerythritol trichlorohydrin - Google Patents
Production of pentaerythritol trichlorohydrinInfo
- Publication number
- GB925467A GB925467A GB32626/61A GB3262661A GB925467A GB 925467 A GB925467 A GB 925467A GB 32626/61 A GB32626/61 A GB 32626/61A GB 3262661 A GB3262661 A GB 3262661A GB 925467 A GB925467 A GB 925467A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pentaerythritol
- trichlorhydrin
- production
- dichlorhydrin
- hydrogen chloride
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/24—Synthesis of the oxirane ring by splitting off HAL—Y from compounds containing the radical HAL—C—C—OY
- C07D301/26—Y being hydrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/34—Halogenated alcohols
- C07C31/36—Halogenated alcohols the halogen not being fluorine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Epoxy Compounds (AREA)
Abstract
A process for the production of pentaerythritol trichlorhydrin comprises dissolving pentaerythritol in a reaction product of pentaerythritol and hydrogen chloride, passing hydrogen chloride in at least the amount theoretically necessary through the resultant solution at a temperature between about 170 DEG to 200 DEG C., at a pressure between atmospheric and about 5 atmos, and recovering the pentaerythritol trichlorhydrin thus produced. Specified pentaerythritol -HCl reaction products are the mono-, di- and trichlorhydrins and 5,5-bischlormethyldioxan-1,3 and mixtures thereof. The effluent HCl may be recirculated after condensation of liquid entrained substances. Batchwise and continuous operation is possible. A series of reaction vessels may be used, the pentaerythritol, preferably dissolved in dichlorhydrin, being chlorinated up to about the dichlorhydrin stage in the first vessel at 130-175 DEG C., and converted to the trichlorhydrin at 170-200 DEG C. in subsequent vessel(s). Specification 764,664 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB59414A DE1129940B (en) | 1960-09-17 | 1960-09-17 | Process for the preparation of pentaerythritol trichlorohydrin |
Publications (1)
Publication Number | Publication Date |
---|---|
GB925467A true GB925467A (en) | 1963-05-08 |
Family
ID=6972459
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32626/61A Expired GB925467A (en) | 1960-09-17 | 1961-09-12 | Production of pentaerythritol trichlorohydrin |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1129940B (en) |
GB (1) | GB925467A (en) |
-
1960
- 1960-09-17 DE DEB59414A patent/DE1129940B/en active Pending
-
1961
- 1961-09-12 GB GB32626/61A patent/GB925467A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE1129940B (en) | 1962-05-24 |
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