GB253542A - Improvements in or relating to the manufacture of synthetic camphor - Google Patents
Improvements in or relating to the manufacture of synthetic camphorInfo
- Publication number
- GB253542A GB253542A GB14666/26A GB1466626A GB253542A GB 253542 A GB253542 A GB 253542A GB 14666/26 A GB14666/26 A GB 14666/26A GB 1466626 A GB1466626 A GB 1466626A GB 253542 A GB253542 A GB 253542A
- Authority
- GB
- United Kingdom
- Prior art keywords
- turpentine
- solvent
- hydrocarbons
- relating
- manufacture
- 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
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/385—Saturated compounds containing a keto group being part of a ring
- C07C49/417—Saturated compounds containing a keto group being part of a ring polycyclic
- C07C49/423—Saturated compounds containing a keto group being part of a ring polycyclic a keto group being part of a condensed ring system
- C07C49/427—Saturated compounds containing a keto group being part of a ring polycyclic a keto group being part of a condensed ring system having two rings
- C07C49/433—Saturated compounds containing a keto group being part of a ring polycyclic a keto group being part of a condensed ring system having two rings the condensed ring system containing seven carbon atoms
- C07C49/437—Camphor; Fenchone
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
253,542. Darrasse, L., Darrasse, E.., and Dupont, L. June 12, 1925, [Convention date]. Bornyl esters.-In a process as described in Specification 164,357, for the production of bornyl esters by heating together turpentine, oxalic acid, and a solvent, simple hydrocarbons such as benzene, toluene, and other hydrocarbons of this series or mixtures thereof are used instead of chlorinated hydrocarbons. As the reaction is slower the relative proportion of solvent used is increased. In an example dry oxalic acid, turpentine, and a mixture of toluene and benzene are heated together, the quantity of solvent being two or three times the quantity of turpentine. Specification 14408/08. [Class 2, Acids and salts, Organic &c.], also is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR253542X | 1925-06-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB253542A true GB253542A (en) | 1927-08-11 |
Family
ID=8884336
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14666/26A Expired GB253542A (en) | 1925-06-12 | 1926-06-10 | Improvements in or relating to the manufacture of synthetic camphor |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB253542A (en) |
-
1926
- 1926-06-10 GB GB14666/26A patent/GB253542A/en not_active Expired
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
S73 | Revocation on comptroller's initiative (section 73/patents act 1977) |
Free format text: PATENT REVOKED; PATENT REVOKED UNDER SECTION 73(2) ON 03 JUNE 2021 |