HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (1-Phenylcyclopentyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Phenylcyclopentane-1-carbaldehyde | HCID 11095124 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1-Phenylcyclopentyl)methanol | HCID 123544 | — |
Reaction Steps
To a stirred solution of 1-phenyl-cyclopentanecarbaldehyde (277) (11.5 g, 71.82 mmol) in methanol (150 mL) was added NaBH4 at 0° C. portion-wise and the reaction was stirred at room temperature for 2 h. After completion of the reaction, the reaction mixture was quenched with a saturated aqueous solution of ammonium chloride (20 mL). Subsequently, the methanol was removed, the residue diluted with water (100 mL) and extracted with ethyl acetate (3×100 mL) and the separated organic part was dried and concentrated. The crude product was purified by Combi-Flash column (eluted at 5-10% ethyl acetate in hexane) to get (1-phenyl-cyclopentyl)-methanol] (278) (10 g, 79.0%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045486B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-fe5ba759481f42868ed98d12c321587e |
| Source note | uspto-grants-2015_06 |