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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668965Generated: October 31, 2026

4-Toluenesulfonyl chloride → N-((4-bromo-5-methylthiophen-2-yl)methyl)-N-(2,2-dimethoxyethyl)-4-methylbenzenesulfonamide

https://huagongshe.com/reaction/1668965

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantN-((4-bromo-5-methylthiophen-2-yl)methyl)-2,2-dimethoxyethanamineHCID 58466475—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-((4-bromo-5-methylthiophen-2-yl)methyl)-N-(2,2-dimethoxyethyl)-4-methylbenzenesulfonamideHCID 58466455—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-((4-bromo-5-methylthiophen-2-yl)methyl)-2,2-dimethoxyethanamine (14.5 g, 49 mmol) was dissolved in DCM (100 ml) and TEA (14 ml, 99 mmol) was added. The reaction was cooled to 0° C. with an ice bath and 4-tosyl chloride (8.5 ml, 59 mmol) was added portionwise. The reaction was allowed to warm up to RT and stirred overnight. The reaction was then diluted with DCM and water. The layers were separated and the organic layer was washed (2×) with an aqueous saturated solution of sodium bicarbonate, then with water and then brine. The organic layer was then dried with sodium sulfate purified by column chromatography on silica gel using a gradient of 30 to 70% EtOAc in hexanes to give N-((4-bromo-5-methylthiophen-2-yl)methyl)-N-(2,2-dimethoxyethyl)-4-methylbenzenesulfonamide as light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989461B2
Source datasetuspto-grants-2011_08
ORD IDord-11fea83281184496822ae7697fb2bddb
Source noteuspto-grants-2011_08