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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084983Generated: October 25, 2026

Water → Acetamide, N-(2-methoxyphenyl)-

https://huagongshe.com/reaction/1084983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant8-HydroxyquinolineHCID 1923—
Reactant2'-BromoacetanilideHCID 136416—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductAcetamide, N-(2-methoxyphenyl)-HCID 7135945.4%

Reaction Steps

Then, 2.14 g of the 2-bromo-1-acetylaminobenzene was added to a solution containing 2.3 ml of a 28% methanol solution of sodium methoxide, 100 mg of cuprous chloride, and 145 mg of 8-hydroxyquinoline in 40 ml of methanol, and the mixture was heated under reflux for 50 minutes. After cooling with water, ethyl acetate was added thereto, and the resulting mixture was washed with water and dried over Glauber's salt. The solvent was distilled off, and the obtained crude crystals were recrystallized from an n-hexane/ethyl acetate solvent mixture, to obtain 1.56 g (yield: 95%) of the desired compound. The spectrum data of the compound was in agreement with the spectrum data of the separately synthesized reference compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05006660
Source datasetuspto-grants-1991_04
ORD IDord-754bd2a780e04efca6334d8b524c3684
Source noteuspto-grants-1991_04