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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209688Generated: October 27, 2026

4-Methoxybenzenesulfonyl chloride → 4-[[4-Methoxybenzenesulfonyl]amino]-4-carbomethoxy-tetrahydrothiopyran

https://huagongshe.com/reaction/2209688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantTriethylamineHCID 8471—
ReactantMethyl 4-aminothiane-4-carboxylate hydrochlorideHCID 22907152—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-[[4-Methoxybenzenesulfonyl]amino]-4-carbomethoxy-tetrahydrothiopyranHCID 22907082—

Reaction Steps

To a solution of 4-amino-4-carbomethoxy-tetrahydrothiopyran hydrochloride (3.1 g, 15.0 mmol) in methylene chloride (75 mL) containing triethylamine (3.5 g, 330.0 mmol) is added 4-methoxybenzenesulfonyl chloride (4.1 g, 20.0 mmol) at room temperature. The reaction mixture is stirred at room temperature for 18 hours. The mixture is diluted with water and the organic layer is removed. The aqueous layer is extracted with diethyl ether and the organic extracts are washed with brine, dried (MgSO4) and the solvent is evaporated. The product is purified by silica gel chromatography (50% ethylacetate/hexanes) to provide 4-[[4-methoxybenzenesulfonyl]amino]-4-carbomethoxy-tetrahydrothiopyran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455258
Source datasetuspto-grants-1995_10
ORD IDord-f4504b46dc484affbb57893e0ba4ac51
Source noteuspto-grants-1995_10