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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927412Generated: October 27, 2026

Sodium borohydride → E-{5-Fluoro-2-[2-(4-methoxyphenyl)vinyl]phenyl}methanol

https://huagongshe.com/reaction/1927412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantE-5-Fluoro-2-[2-(4-methoxyphenyl)vinyl]benzaldehydeHCID 57831341—
SolventMethanolHCID 887—
ProductE-{5-Fluoro-2-[2-(4-methoxyphenyl)vinyl]phenyl}methanolHCID 57831377—

Reaction Steps

1.73 g (45.60 mmol) of sodium borohydride are added in portions to a solution of 7.79 g (30.40 mmol) of E-5-fluoro-2-[2-(4-methoxyphenyl)vinyl]benzaldehyde in 500 ml of methanol at 0° C., and the mixture is stirred at room temperature for 2 hours. After reaction is complete, the mixture is concentrated to dryness and the residue is taken up in water and dichloromethane. The aqueous phase is extracted twice more with dichloromethane. The combined organic phases are dried over sodium sulfate, filtered and concentrated to dryness. The resulting residue is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 4:1→1:1). 6.8 g (85% of theory) of a colorless solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183271B2
Source datasetuspto-grants-2012_05
ORD IDord-bcd22c98731b487abe3938b40b40cdf0
Source noteuspto-grants-2012_05