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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799673Generated: October 30, 2026

Benzenemethanethiol, alpha,alpha-diphenyl- → HCID 68599758, compound

https://huagongshe.com/reaction/1799673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenemethanethiol, alpha,alpha-diphenyl-HCID 77281—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 45121755HCID 45121755—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68599758HCID 68599758—

Reaction Steps

A solution of 2.73 g of 5-ethynyl-4-hydroxymethylthiazole in 65 ml of THF was cooled in ice under an argon atmosphere, and 6.5 g of triphenylmethane thiol and 440 mg of potassium-t-butoxide were added to the cooled solution. The mixture was stirred at room temperature for 2 hr. Brine 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. Ethyl acetate (10 ml) and 10 ml of hexane were added to the residue, and the resultant precipitate was collected by filtration to give 7.26 of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344154B2
Source datasetuspto-grants-2013_01
ORD IDord-357c0af59ae445228ede345e72dc3264
Source noteuspto-grants-2013_01