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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583067Generated: November 2, 2026

Pyridine → 4-(Benzyloxy)-1-(bromomethyl)-2-fluorobenzene

https://huagongshe.com/reaction/1583067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhosphorus tribromideHCID 24614—
Reactant4-Benzyloxy-2-fluorobenzyl alcoholHCID 12136990—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product4-(Benzyloxy)-1-(bromomethyl)-2-fluorobenzeneHCID 15895891—

Reaction Steps

A stirred, cooled (ice bath) solution of 4-benzyloxy-2-fluoro-benzyl alcohol (Compound 9, 15 g, 64.6 mmol) in anhydrous diethyl ether (100 mL) was treated with pyridine (5.75 mL, 71.1 mmol) followed by phosphorus tribromide (6.13 mL, 64.6 mmol). After 90 min. the reaction mixture was diluted with water and extracted with diethyl ether (×2). The combined organic phase was dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford the title product as an oil that solidified on standing (18 g, 89.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06740676B2
Source datasetuspto-grants-2004_05
ORD IDord-295b3181adb64d52ada0ac42230bb43f
Source noteuspto-grants-2004_05