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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465444Generated: November 2, 2026

Trifluoroacetic acid → 4-(4-Ethynyl-1,3-thiazol-2-yl)piperidine

https://huagongshe.com/reaction/1465444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-(4-ethynyl-1,3-thiazol-2-yl)piperidine-1-carboxylateHCID 58181284—
SolventDichloromethaneHCID 6344—
Product4-(4-Ethynyl-1,3-thiazol-2-yl)piperidineHCID 5818126898%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 4-(4-ethynyl-1,3-thiazol-2-yl)piperidine-1-carboxylate (1.87 g, 6.40 mmol) in anhydrous dichloromethane (16 ml) was added at 0° C. trifluoroacetic acid (16 ml). After stirring at 0° C. for 30 mins, the mixture was concentrated under reduced pressure. Saturated aqueous sodium hydrogen carbonate solution was added to the residue, and the mixture was concentrated to dryness. The residue was washed with dichloromethane (extracted from solid phase) and the washing solution was concentrated to give 4-(4-ethynyl-1,3-thiazol-2-yl)piperidine (1.176 g, yield 98%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-63a081dddd814109a91eefcabe8084a6
Source noteuspto-grants-2015_04