GB748287A - Phenol production - Google Patents
Phenol productionInfo
- Publication number
- GB748287A GB748287A GB14105/53A GB1410553A GB748287A GB 748287 A GB748287 A GB 748287A GB 14105/53 A GB14105/53 A GB 14105/53A GB 1410553 A GB1410553 A GB 1410553A GB 748287 A GB748287 A GB 748287A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sulphuric acid
- weight
- per cent
- acetone
- concentration
- 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
- C07C37/08—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by decomposition of hydroperoxides, e.g. cumene hydroperoxide
-
- 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
- C07C39/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring monocyclic with no unsaturation outside the aromatic ring
- C07C39/04—Phenol
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/02—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides
- C07C409/04—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides the carbon atom being acyclic
- C07C409/08—Compounds containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/02—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides
- C07C409/04—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides the carbon atom being acyclic
- C07C409/08—Compounds containing six-membered aromatic rings
- C07C409/10—Cumene hydroperoxide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/53—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of hydroperoxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/04—Saturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/08—Acetone
Abstract
The process of the parent Specification is modified in that the concentration of sulphuric acid in the reaction medium is less than 0.05 per cent by weight. The reaction is preferably carried out in a medium which contains less than one per cent by weight of water, and at a temperature between 50 DEG and 90 DEG C. In examples: (1) a solution of isopropylbenzene hydroperoxide in isopropylbenzene was decomposed to phenol and acetone with a solution of sulphuric acid in acetone, the concentration of sulphuric acid in the reaction mixture being 0.04 per cent by weight; (2) as in (1) the concentration of sulphuric acid being 0.022 per cent by weight; (3) meta-di-isopropylbenzene dihydroperoxide was dissolved in acetone, added to a solution of sulphuric acid in acetone and the mixture refluxed to give resorcinol, the concentration of sulphuric acid being about 0.008 per cent by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB14105/53A GB748287A (en) | 1953-05-20 | 1953-05-20 | Phenol production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB14105/53A GB748287A (en) | 1953-05-20 | 1953-05-20 | Phenol production |
Publications (1)
Publication Number | Publication Date |
---|---|
GB748287A true GB748287A (en) | 1956-04-25 |
Family
ID=10035071
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14105/53A Expired GB748287A (en) | 1953-05-20 | 1953-05-20 | Phenol production |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB748287A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4283570A (en) * | 1976-08-18 | 1981-08-11 | Mitsui Petrochemical Industries Ltd. | Process for preparing resorcinol |
-
1953
- 1953-05-20 GB GB14105/53A patent/GB748287A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4283570A (en) * | 1976-08-18 | 1981-08-11 | Mitsui Petrochemical Industries Ltd. | Process for preparing resorcinol |
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