GB439053A - Production of resorcinol - Google Patents
Production of resorcinolInfo
- Publication number
- GB439053A GB439053A GB15915/34A GB1591534A GB439053A GB 439053 A GB439053 A GB 439053A GB 15915/34 A GB15915/34 A GB 15915/34A GB 1591534 A GB1591534 A GB 1591534A GB 439053 A GB439053 A GB 439053A
- Authority
- GB
- United Kingdom
- Prior art keywords
- resorcinol
- carried out
- temperature
- sulphur trioxide
- production
- 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
- C07C37/01—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis
- C07C37/04—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis by substitution of SO3H groups or a derivative thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
Resorcinol is obtained by sulphonating benzene to the monosulphonic acid with sulphur trioxide in a medium of liquid sulphur dioxide, the reaction being carried out slowly under pressure at a temperature of 10 to 35 DEG C., then converting to the disulphonic acid with a further quantity of sulphur trioxide preferably in the absence of a diluent and at a temperature finally reaching 100 DEG C., and finally hydrolyzing the product directly with alkali metal hydroxide. The resorcinol is isolated by acidifying. The disulphonation is preferably carried out after removal of the solvent. An example of the process described is given.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US439053XA | 1933-05-26 | 1933-05-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB439053A true GB439053A (en) | 1935-11-28 |
Family
ID=21929507
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15915/34A Expired GB439053A (en) | 1933-05-26 | 1934-05-28 | Production of resorcinol |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB439053A (en) |
-
1934
- 1934-05-28 GB GB15915/34A patent/GB439053A/en not_active Expired
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