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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054031Generated: November 2, 2026

Bromoacetyl chloride → HCID 14292484, compound

https://huagongshe.com/reaction/1054031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl chlorideHCID 89602—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(thiophen-2-ylmethyl)anilineHCID 1133193—
SolventDimethylformamideHCID 6228—
ProductHCID 14292484HCID 1429248478.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. stirring suspension of the N-(thiophen-2-ylmethyl)aniline (3.51 g, 18.53 mmol) and sodium bicarbonate (1.71 g, 20.38 mmol) in dimethylformamide (15.0 mL), it was added bromoacetyl chloride (1.54 mL, 18.53 mmol). The ice bath was removed and the flask was attached to a bubbler to allow gas evolution and expansion. The reaction was stirred overnight at room temp. Most of the volatiles were evaporated in vacuo, then the residue was taken up in dichloromethane and was washed with water first and then brine. The resulting organic layer was dried over MgSO4(s) and concentrated. The obtained crude was absorbed under vacuum on Florisil with the aid of DCM (dry load). The obtained dispersion was purified by column chromatography (Biotage system, hex:EtOAc 1-20% gradient over 30 CV, 40 g Silicycle silica column) The collected fractions were evaporated to afford 4.51 g of 2-bromo-N-phenyl-N-(thiophen-2-ylmethyl)acetamide (14.55 mmol; 78%), which was judged more than 97% pure by 1H-NMR analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394287B2
Source datasetuspto-grants-2016_07
ORD IDord-533e2d6eeef949d8a3dc70e82198f8ce
Source noteuspto-grants-2016_07