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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239625Generated: October 31, 2026

4-Fluoroanisole → HCID 53234531, compound

https://huagongshe.com/reaction/239625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluoroanisoleHCID 9987—
ReactantOxalyl chlorideHCID 65578—
ReactantBenzeneacetic acid, 2-fluoro-HCID 67979—
ReactantAluminum(III) ChlorideHCID 6451240—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 53234531HCID 5323453154%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Fluorophenylacetic acid (2.0 g, 13.14 mmoles) was dissolved in 20 ml dichloromethane. To this mixture, oxalylchloride (1.66 g, 13.14 mmoles) and DMF (3 drops) were added at 0° C. and stirred for 30 min. The solvent was evaporated and dissolved in 20 ml dichloromethane. To this mixture, 4-fluoroanisole (1.10 g, 8.76 mmoles) was added and cooled to 0° C. At 0° C. AlCl3 (1.75 g, 13.14 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, 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 (1.17 g, 54% yield. 1H-NMR (δ ppm, DMSO-D6, 400 MHz): δ 11.25(s,1H), 7.73(dd, J=9.5,3.2 Hz, 1H), 7.43(dt, J=8.8,3.1 Hz, 1H), 7.35(d, J=6.2 Hz, 1H), 7.31(d, J=7.2 Hz, 1H), 7.19(d, J=8.2 Hz, 1H), 7.03(dd, J=9.1,4.6 Hz, 1H),4.50(s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642607B2
Source datasetuspto-grants-2014_02
ORD IDord-5c664acc7d6e45039e91a7a56e643026
Source noteuspto-grants-2014_02