HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 21554190, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-([2',3',4',5'-Tetrahydro[1,1'-biphenyl]]-4-yl)ethan-1-one | HCID 21533395 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21554190 | HCID 21554190 | — |
Reaction Steps
A solution of 7 g of sodium borohydride in 300 ml of methanol and 80 ml of water is cooled to 5°C and 50 g of p-(1-cyclohexenyl)-acetophenone are stirred in portionwise. The batch is stirred on for 2 hours at room temperature, the solution is concentrated to half its volume in a rotary evaporator, mixed with 1 litre of water and extracted with 3 × 500 ml of methylenechloride. The methylenechloride residue is recrystallized from petroleum ether and furnishes 1-hydroxy-1-[p-(1-cyclohexenyl)-phenyl]-ethane melting at 60°-62°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03944589 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-edddeffe78554bc3a661b6ad1afebe52 |
| Source note | uspto-grants-1976_03 |