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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637186Generated: October 31, 2026

Acetyl chloride → N-[4-Methoxy-3-(methoxycarbonyl)phenyl]ethanimidic acid

https://huagongshe.com/reaction/637186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 5-amino-o-anisateHCID 89843—
ReactantDichloromethane methanolHCID 21226129—
SolventDichloromethaneHCID 6344—
ProductN-[4-Methoxy-3-(methoxycarbonyl)phenyl]ethanimidic acidHCID 4153338—

Reaction Steps

Alternately, combine methyl 2-methoxy-5-aminobenzoate (1.5 g, 8.3 mmol) and dichloromethane (25 mL). Cool in an ice bath. Add N,N-diisopropylethylamine (3.2 mL, 18.2 mmol), and acetyl chloride (0.62 mL, 9.7 mmol). Warm to ambient temperature. After 4 hours, dilute the reaction mixture with dichloromethane and extract three times with half saturated aqueous ammonium chloride solution. Dry the organic layer over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 3% methanol/dichloromethane/0.1% concentrated aqueous ammonia to give methyl 2-methoxy-5-acetamidobenzoate: mp; 132-134° C. Elemental Analysis calculated for C11H13NO4: C, 59.19; H, 5.87. Found C, 59.04; H, 5.86.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194406B1
Source datasetuspto-grants-2001_02
ORD IDord-4f51ea3bf8f04236bb9d1e0c1bfd8179
Source noteuspto-grants-2001_02