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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239615Generated: November 1, 2026

4-Bromoanisole → HCID 60209026, compound

https://huagongshe.com/reaction/239615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
ReactantOxalyl chlorideHCID 65578—
ReactantBenzeneacetic acid, 2-fluoro-HCID 67979—
ReactantAluminum(III) ChlorideHCID 6451240—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 60209026HCID 6020902681%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Fluorophenylacetic acid (2.96 g, 19.24 mmoles) was dissolved in 50 ml dichloromethane. To this mixture, oxalylchloride (2.1 ml, 24.05 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 (3.0 g, 16.03 mmoles) was added and cooled to 0° C. At 0° C. AlCl3 (3.21 g, 24.05 mmoles) was added and the reaction mixture was warmed to RT and stirred for 12 h. 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 off-white solid (4.0 g, 81% yield. 1H-NMR (δ ppm, CDCl3, 400 MHz): δ 11.97(s,1H), 8.01(d, J=1.7 Hz, 1H), 7.58(dd, J=8.8,2.3.1 Hz, 1H), 7.35(m,1H), 7.23(d, J=7.3 Hz, 1H), 7.17(m, 2H), 6.92(d, J=8.9 Hz, 1H),4.33(s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642607B2
Source datasetuspto-grants-2014_02
ORD IDord-8a5ebf57c8a942f58bfc5441649e8bfd
Source noteuspto-grants-2014_02