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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720642Generated: November 2, 2026

Ethanethiol → HCID 15708214, compound

https://huagongshe.com/reaction/1720642

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 numberUS05506356
Source datasetuspto-grants-1996_04
ORD IDord-0f509fd956074c83953991f49e37ef9c
Source noteuspto-grants-1996_04