HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → 3-Benzylmercapto-4-carbomethoxy benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 3-Benzylmercapto-4-carbomethoxy benzoic acid | HCID 54108258 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium borohydride | HCID 4311764 | — |
| Product | 3-Benzylmercapto-4-carbomethoxy benzyl alcohol | HCID 54409048 | 65.2% |
Reaction Steps
28 ml of boron trifluoride etherate is added to a suspension of 46 g of crude 3-benzylmercapto-4-carbomethoxy benzoic acid in 750 ml of anhydrous tetrahydrofuran and 7 g of sodium borohydride. The reaction mixture is stirred for 3-4 hours at room temperature, then diluted with about 20 ml of 2N hydrochloric acid and 500 ml of water. The product obtained is extracted with ether and the ether extract is washed with water and saturated sodium chloride solution, dried over sodium sulfate and evaporated to dryness. Crystallization from ethyl acetate:hexane (1:2) yielded 28.6 g of 3-benzylmercapto-4-carbomethoxy benzyl alcohol having a melting point of 89.5°-92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04051148 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-ea52d62c84174c999e6a506d1179c345 |
| Source note | uspto-grants-1977_09 |