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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700351Generated: November 2, 2026

Trifluoroacetic acid → 2-Aminoacetanilide

https://huagongshe.com/reaction/1700351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl n-[(phenylcarbamoyl)methyl]carbamateHCID 10634424—
SolventDichloromethaneHCID 6344—
Product2-AminoacetanilideHCID 208384—

Reaction Steps

40 ml of dichloromethane and 20 ml of trifluoroacetic acid were added to 687 mg (2.74 mmol) of t-butyl phenylcarbamoylmethylcarbamate, and they were stirred at room temperature for 3 hours. Dichloromethane and trifluoroacetic acid were evaporated under reduced pressure. A saturated aqueous sodium hydrogencarbonate solution was added to the residue. After the extraction with ethyl acetate and then with dichloromethane, the organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350762B1
Source datasetuspto-grants-2002_02
ORD IDord-3e3152f295594a38a18d8080cd3cea7e
Source noteuspto-grants-2002_02