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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7403Generated: October 26, 2026

Triethylamine → 3-Methyl-n-(1-methylethyl)-2-[(1-oxo-2-propenyl)amino]benzamide

https://huagongshe.com/reaction/7403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant2-amino-3-methyl-N-(1-methylethyl)benzamideHCID 16776093—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
Product3-Methyl-n-(1-methylethyl)-2-[(1-oxo-2-propenyl)amino]benzamideHCID 2199084752.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the title compound of Step B (0.93 g, 4.8 mmol) in dichloromethane (10 mL) was added triethylamine (0.876 mL, 6.2 mmol) and the mixture was cooled to 0° C. Acryloyl chloride (0.433 mL, 5.3 mmol) was then added and the mixture was warmed to ambient temperature and stirred overnight. Dimethylaminopyridine (1.0 g, 7.7 mmol) was then added followed by acryloyl chloride (0.475 mL, 5.8 mmol). The mixture was stirred at ambient temperature for 0.5 h before being diluted with 1N HCl and extracted twice with dichloromethane. The organic extracts were dried (MgSO4) and concentrated to give the product of Step C (0.62 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087598B2
Source datasetuspto-grants-2006_08
ORD IDord-a657f347ef0e49a29c12131dbb390714
Source noteuspto-grants-2006_08