HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 67177503, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86638535 | HCID 86638535 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67177503 | HCID 67177503 | — |
Reaction Steps
To a stirred, cooled (0° C.) solution of sodiumborohydride (1.0 g) in methanol (20 ml) under an argon atmosphere was added slowly a solution of [1-(3,5-difluoro-phenyl)cyclopropyl]-acetaldehyde in methanol (10 ml). Stirring was continued at room temperature overnight, then the reaction mixture was quenched by slow addition of water. Methanol was evaporated and the aqueous phase was extracted with ethyl acetate twice. The combined organic layers were dried over MgSO4 and concentrated to give 2-[1-(3,5-difluoro-phenyl)-cyclopropyl]-ethanol as yellow liquid (2.37 g). 1H-NMR (300 MHz, CDCl3, δ): 0.76-0.86 (m, 4H), 1.85 (t, J=7 Hz, 2H), 3.61-3.62 (m, 2H), 6.60-6.67 (m, 1H), 6.78-6.85 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357712B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-a2db7186d4fd405dbc804a7229d2a660 |
| Source note | uspto-grants-2013_01 |