HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-Chloro-4-cyclohexylpropiolic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl alpha,beta-dibromo-beta-(3-chloro-4-cyclohexyl)propionate | HCID 57052243 | — |
| Product | 3-Chloro-4-cyclohexylpropiolic acid | HCID 70542015 | — |
Reaction Steps
Powdered ethyl α,β-dibromo-β-(3-chloro-4-cyclohexyl)propionate (33.0 g.) is added portion-wise to 20% ethanolic potassium hydroxide (135 ml) at room temperature. The mixture is refluxed on a steam bath for 6 hours. The alcohol is evaporated and the residue is dissolved in water and covered with ether and is acidified with cold, dilute hydrochloric acid. The ether layer is washed with water, saline, and dried over sodium sulfate. The ether is removed to give a residue which is triturated with carbon tetrachloride. Recrystallization is carried out from acetic acid-water. This material is digested and triturated with boiling carbon tetrachloride to give 3-chloro-4-cyclohexylpropiolic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04166133 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-0b19a350062c4f358df6b9a30136811a |
| Source note | uspto-grants-1979_08 |