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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030001Generated: October 26, 2026

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

https://huagongshe.com/reaction/1030001

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 numberUS05104414
Source datasetuspto-grants-1992_04
ORD IDord-f29c70e8284d432d93209922d4ffd944
Source noteuspto-grants-1992_04