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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672631Generated: October 26, 2026

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

https://huagongshe.com/reaction/1672631

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 5783137786.6%

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 from Example 29A 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 then taken up in water and dichloromethane. The aqueous phase is then 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% yield) of a colorless solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998988B2
Source datasetuspto-grants-2011_08
ORD IDord-2972fe19eb314e09a9e1aadfd3b50740
Source noteuspto-grants-2011_08