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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476148Generated: October 31, 2026

4-Bromoanisole → HCID 53234358, compound

https://huagongshe.com/reaction/1476148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
Reactant2-(4-Fluorophenyl)acetic acidHCID 9837—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 53234358HCID 5323435837%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Fluoro phenylacetic acid (12.3 g, 79.79 mmoles) was dissolved in 30 ml dichloromethane. To this mixture, oxalylchloride (10.17 g, 79.79 mmoles) and DMF (3 drops) were added at 0° C. and stirred for 30 min. The solvent was evaporated and dissolved in 30 ml dichloromethane. To this mixture, 4-bromoanisole (10 g, 53.47 mmoles) was added and cooled to 0° C. At 0° C. AlCl3 (10.6 g, 79.79 mmoles) was added and the reaction mixture was warmed to RT and stirred overnight. The reaction mixture was quenched by the addition of 2N HCl and extracted with ethyl acetate, dried over sodium sulphate and concentrated. The crude product was purified by column chromatography with ethyl acetate:petroleum ether to afford the title compound as white solid (6.1 g, 37% yield. 1H-NMR (δ ppm, CDCl3, 400 MHz): δ 12.05(s,1H), 7.96(d, J=2.3Hz, 1H), 7.58(dd, J=8.9, 2.4Hz, 1H), 7.24(dt, J=5.4, 1.9Hz, 2H), 7.09(dt, J=8.6, 2.1Hz, 2H),6.79(d, J=8.7Hz, 1H), 4.27(s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018375B2
Source datasetuspto-grants-2015_04
ORD IDord-d28c2044d02e4ccda8d829c825cd5c85
Source noteuspto-grants-2015_04