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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465653Generated: October 31, 2026

4-Methoxybenzenethiol → HCID 58442390, compound

https://huagongshe.com/reaction/1465653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzenethiolHCID 12765—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 58442513HCID 58442513—
CatalystHCID 178419072HCID 178419072—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58442390HCID 5844239090%

Reaction Steps

A mixture of 1-(4-iodo-2,6-dimethylphenyl)ethanone (1.5 g, 5.5 mmol, 1.0 equiv), 4-methoxybenzenethiol (1.01 mL, 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-(4-(4-methoxyphenylthio)-2,6-dimethylphenyl)ethanone (1.41 g, 4.9 mmol) as yellow oil in 90% yield: 1H NMR (DMSO-d6, 500 MHz) δ 7.39 (d, J=8.5 Hz, 2 H), 6.96 (d, J=8.5 Hz, 2 H), 6.79 (s, 2 H), 3.82 (s, 3 H), 2.43 (s, 3 H), 2.13 (s, 6 H); ESI-MS: m/z 287.6 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999983B2
Source datasetuspto-grants-2015_04
ORD IDord-16c09d40020a4e1a96f21bbde67c7d99
Source noteuspto-grants-2015_04