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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261300Generated: October 27, 2026

Propargyl alcohol → Ethyl 2-(2-propynyloxy)-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/2261300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 2-chlorothiazole-4-carboxylateHCID 13106141—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(2-propynyloxy)-1,3-thiazole-4-carboxylateHCID 5773633859.9%

Reaction Steps

0.20 g of propargyl alcohol was dissolved in 20 ml of tetrahydrofuran, and 0.13 g of 60% sodium hydride was added at room temperature. The mixture was stirred at room temperature for 1 hour. After 0.50 g of ethyl 2-chloro-1,3-thiazole-4-carboxylate was added, the reaction mixture was stirred at room temperature for 3 hours. After aqueous saturated ammonium chloride was added, the reaction mixture was extracted with methyl-t-butyl ether. The organic layer was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.33 g of ethyl 2-(2-propynyloxy)-1,3-thiazole-4-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846956B2
Source datasetuspto-grants-2010_12
ORD IDord-43a0b3afc9774a9f938458318588db7d
Source noteuspto-grants-2010_12