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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32817Generated: October 30, 2026

Trifluoroacetic acid → 1-(2-Amino-1,3-thiazol-4-yl)propan-1-one

https://huagongshe.com/reaction/32817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl (4-propionylthiazol-2-yl)carbamateHCID 45117897—
SolventDichloromethaneHCID 6344—
Product1-(2-Amino-1,3-thiazol-4-yl)propan-1-oneHCID 4512169275.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

(4-Propionyl-thiazol-2-yl)-carbamic acid tert-butyl ester (5.0 g, 19.5 mmol) was suspended in dichloromethane (100 mL) at 0° C. Trifluoroacetic acid (100 mL) was added and the mixture was stirred at 0° C. for 1.5 hours. The cooling bath was removed and stirring was continued for 1 hour prior to concentration of the reaction mixture in vacuo. The residue was triturated with ether and filtered. The solid was dissolved in a mixture of dichloromethane and saturated aqueous sodium bicarbonate solution. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The combined organic extracts were washed with brine, dried over sodium sulfate and evaporated to give 1-(2-amino-thiazol-4-yl)-propan-1-one (2.3 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427635B2
Source datasetuspto-grants-2008_09
ORD IDord-131e9f6cf7aa489aaba0f33c4226b354
Source noteuspto-grants-2008_09