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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903681Generated: November 3, 2026

Propargyl bromide → Propargyl 2-chloro-4-trifluoromethyl-5-thiazolecarboxylate

https://huagongshe.com/reaction/1903681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantDiisopropylamineHCID 7912—
Reactant2-Chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylic acidHCID 13282743—
SolventDichloromethaneHCID 6344—
ProductPropargyl 2-chloro-4-trifluoromethyl-5-thiazolecarboxylateHCID 13670344—

Reaction Steps

A mixture of 4.63 g (0.02 mole) of 2-chloro-4-trifluoromethyl-5-thiazolecarboxylic acid, 2.42 g (0.02 mole) of propargyl bromide, 2.59 g (0.02 mole) of diisopropylamine, and 50 ml. of methylene chloride was stirred for 16 hours. The methylene chloride solution was washed successively with diluted hydrochloric acid and saturated sodium bicarbonate, dried (MgSO4) and concentrated under reduced pressure. The residue was Kugelrohr distilled to give propargyl 2-chloro-4-trifluoromethyl-5-thiazolecarboxylate as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04437876
Source datasetuspto-grants-1984_03
ORD IDord-e080420f98a44d219a38df5b6962ff45
Source noteuspto-grants-1984_03