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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050758Generated: October 27, 2026

Benzene → 2-Methyl-4-methoxy-5-fluoroacetylaminophenol

https://huagongshe.com/reaction/2050758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantMethyl fluoroacetateHCID 9959—
ReactantPhenol, 5-amino-4-methoxy-2-methyl-HCID 10197787—
ReactantSodium MethoxideHCID 10942334—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Methyl-4-methoxy-5-fluoroacetylaminophenolHCID 1982115113.9%

Reaction Steps

Into 15 ml of benzene were added 2.10 g (13.7 mmol) of 2-methyl-4-methoxy-5-aminophenol, 1.28 g (13.9 mmol, 1.0 eq.) of methyl fluoroacetate and 1.64 g (30.4 mmol) of sodium methoxide and the mixture was heated under reflux for 6.5 hours. After allowing to cool, the mixture was poured into 300 ml of water, and neutralized with acetic acid and extracted with 200 ml of ethyl acetate. The organic layer was washed with a saturated aqueous solution of common salt and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain dark-brown crystals. The crystals were purified by silica gel column chromatography (Silica Gel 60, trade name, manufactured by Merck Co., 70-230 mesh, 200 g, eluent: ethyl acetate) and pale brown solid matters were obtained from the 600-900 ml fraction. The solid matters were recrystallized from the solvent mixture of hexane/ethyl acetate (2:1 by volume) to give 230 mg (1.9 mmol) of 2-methyl-4-methoxy-5-fluoroacetylaminophenol. The yield was 8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015260
Source datasetuspto-grants-1991_05
ORD IDord-6c2f16e27b4d4939a721ec34b2c80c96
Source noteuspto-grants-1991_05