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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807942Generated: October 31, 2026

Sodium borohydride → HCID 67177503, compound

https://huagongshe.com/reaction/1807942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86638535HCID 86638535—
SolventMethanolHCID 887—
ProductHCID 67177503HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357712B2
Source datasetuspto-grants-2013_01
ORD IDord-a2db7186d4fd405dbc804a7229d2a660
Source noteuspto-grants-2013_01