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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691558Generated: October 27, 2026

Pyridine → 3-Methyl-1-phenylsulfanyl-butan-2-one

https://huagongshe.com/reaction/1691558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThiophenolHCID 7969—
Reactant1-Bromo-3-methylbutan-2-oneHCID 10899037—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product3-Methyl-1-phenylsulfanyl-butan-2-oneHCID 551265—

Reaction Steps

To a solution of thiophenol (4.44 mL; 43.4 mmol) in diethyl ether (29 mL) was added pyridine (17.2 mL; 0.21 mol), followed by the drop-wise addition of a solution of compound 563-B (7.18 g; 43.5 mmol) in diethyl ether (15 mL), at ambient temperature, and the reaction was stirred for 72 h. The reaction was diluted with EtOAc, washed with 2N HCl, H2O, brine, dried over Na2SO4, filtered and the solvent evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO2) eluting with a heptane-EtOAc gradient to afford compound 563-C as an oil. 1H-NMR (CDCl3): δ 1.09-1.10 (d, 6H), 2.90-2.97 (m, 1H), 3.75 (s, 2H), 7.18-7.35 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153682B2
Source datasetuspto-grants-2012_04
ORD IDord-0b1e411e569642f78af07426bafff1e3
Source noteuspto-grants-2012_04