HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-(4-Biphenylyl)-2-butenoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-(4-Biphenylyl)-2-butenoic acid ethyl ester | HCID 54501672 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(4-Biphenylyl)-2-butenoic acid | HCID 296753 | — |
Reaction Steps
The product resulting from (a), above, is mixed with 6 g of 85% potassium hydroxide in 100 ml of aqueous ethanol and the resulting mixture heated on a steam bath for 30 minutes. The mixture is then cooled, poured into ice and extracted thrice with 25 ml portions of diethylether. The aqueous phase is filtered over Celite and the filtrate acidified with 2 N hydrochloric acid to pH 4 and cooled. The resulting precipitate is filtered, washed with ether, air dried with suction and then dried under high vacuum at 50° C. to yield the heading compound, substantially in trans form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04344966 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-adad65625ed443a585f437e7219331b8 |
| Source note | uspto-grants-1982_08 |