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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582637Generated: November 1, 2026

Benzyl Bromide → Benzaldehyde, 2-fluoro-3-(phenylmethoxy)-

https://huagongshe.com/reaction/1582637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2-Fluoro-3-hydroxybenzaldehydeHCID 587789—
SolventDimethylformamideHCID 6228—
ProductBenzaldehyde, 2-fluoro-3-(phenylmethoxy)-HCID 561331—

Reaction Steps

2-Fluoro-3-hydroxybenzaldehyde (16.49 g) was dissolved in dimethylformamide (200 ml) and stirred under an argon atmosphere. Sodium hydride was added (60% in mineral oil, 5.18 g) and the mixture was stirred for 30 minutes. Benzyl bromide was added (16.8 ml) and the mixture was stirred overnight. Reaction mixture was concentrated in vacuo and the resulting residue was partitioned between diethyl ether (200 ml) and water (200 ml). Combined organic extracts were washed with water (400 ml), dried (MgSO4) and concentrated in vacuo. The residue was purified by flash column chromatography, using a gradient of 0-10% ethyl acetate/iso-hexane as eluent to give the product as a yellow solid (18.41 g) 1H NMR (DMSO-d6) δ 5.20(s, 2H), 7.2-7.6(m, 8H), 10.21(s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737435B1
Source datasetuspto-grants-2004_05
ORD IDord-6ab7ebf8c70946518e77e3cc89b83c8c
Source noteuspto-grants-2004_05