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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893115Generated: October 29, 2026

Ethanethiol → HCID 15708214, compound

https://huagongshe.com/reaction/893115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantHCID 22418871HCID 22418871—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthyl AcetateHCID 8857—
ProductHCID 15708214HCID 1570821485%

Reaction Steps

597 mg of ethyl 2-(4-quinolylmethyl)acrylate was dissolved in 3 ml of ethylmercaptan. Then, 50 mg of potassium tert-butoxide was added thereto, and the mixture was stirred at room temperature for two hours. Then, the reaction solution was diluted with 60 ml of ethyl acetate and washed with 40 ml of water and then with 40 ml of a saturated sodium chloride aqueous solution. The organic layer was separated, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residual syrup was purified by silica gel column chromatography (n-hexane/ethyl acetate=5/2) and dried to obtain 640 mg (yield: 85%) of the desired product as syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05122523
Source datasetuspto-grants-1992_06
ORD IDord-99a63eb89de54d82b71404bc9661e4f0
Source noteuspto-grants-1992_06