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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 3-Acetyl-4-methoxyacetanilide | HCID 2817418 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Dimethylamino-1-(2'-methoxy-5'-acetamidophenyl)prop-2-en-1-one | HCID 66603430 | 101.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812176B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-662f99a291d04c5db5a170b694992c61 |
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| Source note | uspto-grants-2010_10 |
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