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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159494Generated: November 1, 2026

Dimethylformamide dimethyl acetal → 3-Dimethylamino-1-(2'-methoxy-5'-acetamidophenyl)prop-2-en-1-one

https://huagongshe.com/reaction/1159494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant3-Acetyl-4-methoxyacetanilideHCID 2817418—
SolventEthanolHCID 702—
Product3-Dimethylamino-1-(2'-methoxy-5'-acetamidophenyl)prop-2-en-1-oneHCID 66603430101.4%

Reaction Conditions

Temperature22 °C

Reaction Steps

Dimethylformamide dimethyl acetal (693.3 g) was added to a suspension of 2′-methoxy-5′-acetamidoacetophenone (3, 1215.1 g) in ethanol (12.15 L) stirred under nitrogen at 22° C. After the resulting suspension had been stirred and refluxed under nitrogen for 18 hours, all solids had dissolved, and additional dimethylformamide dimethyl acetal (346.2 g) was added to the homogeneous reaction mixture. Stirring and refluxing under nitrogen were continued for an additional 30 hours, after which additional dimethylformamide dimethyl acetal (346.2 g) was added. The reaction mixture was then stirred and refluxed under nitrogen for a final 17.5 hours, after which the reaction mixture was rotary evaporated at <45° C. and <50 mm HgA to a solid residue that was dried further overnight at <45° C. and <1 mm HgA to provide brown solid 4 (1547.9 g, 100.6% yield). LC/MS analyses revealed 98.3% and 100% conversion of 3 to 4 before and after evaporation of solvent, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812176B2
Source datasetuspto-grants-2010_10
ORD IDord-662f99a291d04c5db5a170b694992c61
Source noteuspto-grants-2010_10