Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7427Generated: October 25, 2026

3-Fluoro-p-anisaldehyde → 3-Fluoro-4-methoxybenzyl alcohol

https://huagongshe.com/reaction/7427

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-p-anisaldehydeHCID 67696—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3-Fluoro-4-methoxybenzyl alcoholHCID 2774550100%

Reaction Steps

To a solution of 3-fluoro-4-methoxybenzaldehyde (1 g, 6.5 mmol) in methanol (15 mL) was added under ice-cooling sodium borohydride (378 mg, 10 mmol) and the mixture was stirred at room temperature for 1 h. The solvent was evaporated under reduced pressure and the obtained residue was dissolved in ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give an almost pure title compound (1 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087597B1
Source datasetuspto-grants-2006_08
ORD IDord-731e44cf7bd248f291c99babee57228d
Source noteuspto-grants-2006_08