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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303472Generated: November 1, 2026

4-Methoxybenzenethiol → HCID 12043581, compound

https://huagongshe.com/reaction/2303472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzenethiolHCID 12765—
ReactantSodium hydrideHCID 24758—
ReactantHCID 86585614HCID 86585614—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12043581HCID 1204358138.6%

Reaction Steps

A stirring solution of 14 (0.25 g) and 4-methoxybenzenethiol (0.4 g) in THF (20 mL) and DMF (5 mL) was treated with NaH (0.080 g). After 3 h, the reaction was quenched by careful addition of H2O, then diluted with 1:1 EtOAc/hexanes. The organic layer was washed with saturated aqueous NaHCO3, washed with water, washed with brine, dried (MgSO4), filtered, and evaporated. Chromatography (silica gel, 20:80 to 33:67 EtOAc/hexanes) gave 0.11 g of 6-methanesulfonyl-3-(4-methoxyphenylsulfanyl)-benzofuran-2-carbonitrile 35 as a solid; (m+H)+ 360.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433005B1
Source datasetuspto-grants-2002_08
ORD IDord-4015d596514b49e1a804c35642de0973
Source noteuspto-grants-2002_08