GB760341A - 2-hydroxy-3:5:6-trichlorobenzyl alcohol - Google Patents
2-hydroxy-3:5:6-trichlorobenzyl alcoholInfo
- Publication number
- GB760341A GB760341A GB3240153A GB3240153A GB760341A GB 760341 A GB760341 A GB 760341A GB 3240153 A GB3240153 A GB 3240153A GB 3240153 A GB3240153 A GB 3240153A GB 760341 A GB760341 A GB 760341A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkali
- hydroxide
- hydroxy
- trichlorophenol
- formaldehyde
- 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
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
- C07C37/20—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms using aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/24—Halogenated derivatives
- C07C39/245—Halogenated derivatives monocyclic polyhydroxylic containing halogens bound to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises 2-hydroxy-3,5,6-trichlorobenzyl alcohol, which is prepared by reacting 2,4,5-trichlorophenol with formaldehyde in the presence of an alkali. The alkali may be an alkali metal carbonate or hydroxide or an alkaline earth metal oxide or hydroxide. In examples of the preparation alkalis used are sodium hydroxide, sodium carbonate and calcium hydroxide. The reaction is carried out by heating the trichlorophenol and formaldehyde in an aqueous solution of the alkali. Specification 760,342 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3240153A GB760341A (en) | 1953-11-23 | 1953-11-23 | 2-hydroxy-3:5:6-trichlorobenzyl alcohol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3240153A GB760341A (en) | 1953-11-23 | 1953-11-23 | 2-hydroxy-3:5:6-trichlorobenzyl alcohol |
Publications (1)
Publication Number | Publication Date |
---|---|
GB760341A true GB760341A (en) | 1956-10-31 |
Family
ID=10338049
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3240153A Expired GB760341A (en) | 1953-11-23 | 1953-11-23 | 2-hydroxy-3:5:6-trichlorobenzyl alcohol |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB760341A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3456020A (en) * | 1967-11-28 | 1969-07-15 | Centerchem Inc | Production of 2,2'-methylene bis(3,4,6-trichlorophenol) |
-
1953
- 1953-11-23 GB GB3240153A patent/GB760341A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3456020A (en) * | 1967-11-28 | 1969-07-15 | Centerchem Inc | Production of 2,2'-methylene bis(3,4,6-trichlorophenol) |
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