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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525879Generated: November 2, 2026

Acetic Anhydride → 4-Bromo-2-fluorophenethyl acetate

https://huagongshe.com/reaction/1525879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Bromo-2-fluorobenzeneethanolHCID 53660694—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product4-Bromo-2-fluorophenethyl acetateHCID 7127111790.3%

Reaction Steps

A solution of 2-(4-bromo-2-fluorophenyl)ethanol (3.01 mmol) in dichloromethane (5 mL) and pyridine (10 mL) was treated with 4-(dimethylamino)pyridine (0.151 mmol) and acetic anhydride (9.04 mmol). The reaction was stirred overnight at room temperature. At this point the reaction was diluted with dichloromethane (100 mL). The organic layer was washed three times with 1N aq HCl, once with saturated aq sodium bicarbonate, and once with brine. The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to afford the title compound as a pale beige oil (710 mg, 81% yield). 1H NMR (400 MHz, DMSO-d6) d ppm 1.96 (s, 3 H) 2.90 (t, J=6.44 Hz, 2 H) 4.20 (t, J=6.57 Hz, 2 H) 7.26-7.43 (m, 2 H) 7.51 (dd, J=9.73, 1.89 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09084794B2
Source datasetuspto-grants-2015_07
ORD IDord-bcd694fadea24b7a842dc9c9bac530f6
Source noteuspto-grants-2015_07