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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414135Generated: November 3, 2026

Hydrochloric Acid → N-(2,6-Dimethylphenyl)-2-methoxy-N-(tetrahydro-2-oxo-3-furanyl)acetamide

https://huagongshe.com/reaction/2414135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethoxyacetyl chlorideHCID 96623—
Reactant3-(2,6-Dimethylanilino)oxolan-2-oneHCID 12491481—
SolventO-XyleneHCID 7237—
ProductN-(2,6-Dimethylphenyl)-2-methoxy-N-(tetrahydro-2-oxo-3-furanyl)acetamideHCID 15500995%

Reaction Conditions

Temperature20 °C

Reaction Steps

Over 2 hours, 113 g (1.04 moles) of methoxyacetyl chloride are added at 60°-70° C. and under a pressure of 70°-80 mbar to a suspension of 205 g (1.0 mole) of N-(2-oxotetrahydro-3-furyl)-2,6-dimethylaniline in 500 ml of xylene. Towards the end of the addition of methoxyacetyl chloride the reaction mixture begins to boil, with hydrogen chloride gas evolving. When the addition of methoxyacetyl chloride is complete, the reaction mixture is stirred for 3 hours under weak reflux at 60°-65° C. and under a pressure of 70-80 mbar, and the hydrogen chloride evolving during the reaction is removed. Subsequently, half of the xylene is distilled off, the reaction mixture is cooled to 20° C., the precipitated product is filtered off, washed with xylene and dried, affording 263 g (95% of theory) of N-methoxyacetyl-N-(2-oxotetrahydro-3-furyl)-2,6-dimethylaniline with a melting point of 118°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04721797
Source datasetuspto-grants-1988_01
ORD IDord-c19cd5891c264a74b10e2a58208b4cba
Source noteuspto-grants-1988_01