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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480709Generated: October 30, 2026

4-Methylbenzenethiol → HCID 58442533, compound

https://huagongshe.com/reaction/1480709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylbenzenethiolHCID 7811—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 58442513HCID 58442513—
CatalystHCID 178419072HCID 178419072—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58442533HCID 5844253379%

Reaction Steps

A mixture of 1-(4-iodo-2,6-dimethylphenyl)ethanone (1.5 g, 5.5 mmol, 1.0 equiv), 4-methylbenzenethiol (1.02 g, 8.2 mmol, 1.5 equiv), copper(I) oxide (39.2 mg, 0.3 mmol, 0.05 equiv), and potassium hydroxide (614.1 mg, 11.0 mmol, 2.0 equiv) in DMF (4.4 mL) and H2O (1.1 mL) was heated at reflux for 20 h. The mixture was quenched with H2O (10 mL) and extracted with ether (2×20 mL). The organic layer was collected, dried over MgSO4(s), and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (3.0% EtOAc in hexanes as eluant) to provide 1-(2,6-dimethyl-4-(p-tolylthio)phenyl)ethanone (1.16 g, 4.3 mmol) as yellow oil in 79% yield: 1H NMR (CD3OD, 500 MHz) δ 7.29 (d, J=8.0 Hz, 2H), 7.20 (d, J=8.0 Hz, 2H), 6.88 (s, 2H), 2.45 (s, 3H), 2.35 (s, 3H), 2.15 (s, 6H); ESI-MS: m/z 271.8 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409902B2
Source datasetuspto-grants-2016_08
ORD IDord-4b51eff125a74a1a8ccaee5e4bf270c2
Source noteuspto-grants-2016_08