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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167829Generated: November 2, 2026

3'-Aminoacetophenone → HCID 4054491, compound

https://huagongshe.com/reaction/1167829

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3'-AminoacetophenoneHCID 7417—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant5-Chloro-2-thiophenecarboxylic acidHCID 95048—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 4054491HCID 405449181%

Reaction Steps

Oxalyl chloride (4.9 mL, 56.00 mmol) was added to solution of 5-chloro-thiophene-2-carboxylic acid (4.78 g, 29.40 mmol), DMF (0.25 mL), and CH2Cl2 (50 ml) at room temperature. After stirring overnight, the reaction was stripped of solvent and unreacted oxalyl choride in vacuo, giving a colorless oil. The oil was dissolved in CH2Cl2 (50 mL), and treated with 3-aminoacetophenone (3.78 g, 28.00 mmol) and triethylamine (4.68 mL, 33.60 mmol). After stirring for 1 h, the mixture was diluted with 800 mL of ethyl acetate, extracted with 1N HCl, 1N NaHCO3, brine, and dried over MgSO4. The resulting solution was concentrated in vacuo to a volume of 100 mL, giving 5-chloro-thiophene-2-carboxylic acid (3-acetyl-phenyl)-amide as a white powder, which was collected by filtration and dried under high vacuum (8.12 g, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620828B2
Source datasetuspto-grants-2003_09
ORD IDord-ac1e8753548a47fc879c348d71a688ba
Source noteuspto-grants-2003_09