GB388737A - Normal heptyl phenol and process for the production thereof - Google Patents
Normal heptyl phenol and process for the production thereofInfo
- Publication number
- GB388737A GB388737A GB2165731A GB2165731A GB388737A GB 388737 A GB388737 A GB 388737A GB 2165731 A GB2165731 A GB 2165731A GB 2165731 A GB2165731 A GB 2165731A GB 388737 A GB388737 A GB 388737A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenol
- heptyl
- production
- chloride
- heptyl phenol
- 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
- C07C37/16—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 by condensation involving hydroxy groups of phenols or alcohols or the ether or mineral ester group derived therefrom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
n-Heptyl phenol is obtained by condensing n-heptyl alcohol with phenol in the presence of a condensing agent, such as zinc chloride, calcium chloride, magnesium chloride or anhydrous sodium sulphate, and fractionally distilling the mixture under reduced pressure. The product, which appears to be a mixture of the o-, m- and p-heptyl phenols, has antiseptic properties. In an example, n-heptyl alcohol is prepared in the known manner by destructive distillation of castor oil and reduction of the nanthol obtained, and is then condensed with phenol with the aid of zinc chloride.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2165731A GB388737A (en) | 1931-07-29 | 1931-07-29 | Normal heptyl phenol and process for the production thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2165731A GB388737A (en) | 1931-07-29 | 1931-07-29 | Normal heptyl phenol and process for the production thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
GB388737A true GB388737A (en) | 1933-02-28 |
Family
ID=10166609
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2165731A Expired GB388737A (en) | 1931-07-29 | 1931-07-29 | Normal heptyl phenol and process for the production thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB388737A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2288723A1 (en) * | 1974-10-22 | 1976-05-21 | Mitsubishi Gas Chemical Co | PROCEDURE FOR THE SELECTIVE ALKYLATION OF THE ORTHO POSITION OF THE PHENOLS |
-
1931
- 1931-07-29 GB GB2165731A patent/GB388737A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2288723A1 (en) * | 1974-10-22 | 1976-05-21 | Mitsubishi Gas Chemical Co | PROCEDURE FOR THE SELECTIVE ALKYLATION OF THE ORTHO POSITION OF THE PHENOLS |
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