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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799679Generated: October 27, 2026

Ammonium Chloride → 4-methoxycarbonyl-2-((Z)-2-tritylthioethen-1-yl)thiazole

https://huagongshe.com/reaction/1799679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzenemethanethiol, alpha,alpha-diphenyl-HCID 77281—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-Ethynyl-4-methoxycarbonylthiazoleHCID 86609811—
SolventTetrahydrofuranHCID 8028—
Product4-methoxycarbonyl-2-((Z)-2-tritylthioethen-1-yl)thiazoleHCID 6860112258.5%

Reaction Steps

2-Ethynyl-4-methoxycarbonylthiazole (2.50 g) was dissolved in 70 ml of THF. Triphenylmethylmercaptan (4.96 g) and 336 mg of potassium-t-butoxide were added to the solution at −60° C. under an argon atmosphere. The mixture was stirred at the same temperature for one hr. An aqueous ammonium chloride solution was added to the reaction solution, and the mixture was extracted twice with ethyl acetate. The organic layers were combined, were washed with brine, were then dried over anhydrous magnesium sulfate, were filtered, and were concentrated under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1). Ethyl acetate and hexane were added to a crude product containing a target compound, and the precipitate was collected by filtration to give 3.88 g of 4-methoxycarbonyl-2-((Z)-2-tritylthioethen-1-yl)thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344154B2
Source datasetuspto-grants-2013_01
ORD IDord-c7a663b519d343149c65b7ebaf0aadc0
Source noteuspto-grants-2013_01