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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389793Generated: October 31, 2026

Ethanol → Alpha-(4-Picolylthio)acetophenone

https://huagongshe.com/reaction/1389793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPhenacyl bromideHCID 6259—
ReactantSodium MethoxideHCID 10942334—
ReactantPyridin-4-ylmethanethiolHCID 13092602—
SolventDiethyl EtherHCID 3283—
ProductAlpha-(4-Picolylthio)acetophenoneHCID 13490316—

Reaction Steps

Under a nitrogen atmosphere, sodium methoxide (0.81 g., 15 mmoles) was dissoled in 17.9 ml. of stirring absolute ethanol, and cooled in an ice bath. 4-Picolyl mercaptan (1.88 g., 15 mmoles) in 3 ml. of absolute ethanol was added dropwise over approximately 5 minutes, followed by alpha-bromoacetophenone (3.05 g., 15 mmoles) in 10 ml. of warm absolute ethanol added over approximately 10 minutes. The stirring reaction mixture was warmed to room temperature and left to stir for 17 hours. Salts were removed by filtration through diatomaceous earth, and the solids repulped for 0.5 hour with additional ethanol and refiltered. The ethanol filtrates were combined and concentrated to yield a waxy solid. The waxy solid was taken up in approximately 11 volumes of diethyl ether, treated with activated carbon, filtered and the mother liquor concentrated to a solid (1.90 g.). Recrystallization from diethyl ether/hexane gave purified alpha-(4-picolylthio)acetophenone (1.25 g. in two crops, m.p. 55°-59° C., ir (KBr): 5.92, 6.18, 7.00, 7.76, 9.78, 12.38, 13.70μ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04246263
Source datasetuspto-grants-1981_01
ORD IDord-caecff7706174e06bbbc4caf00b03ba3
Source noteuspto-grants-1981_01