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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254436Generated: October 30, 2026

4-Toluenesulfonyl chloride → N-(2,2-Dimethoxy-ethyl)4-methyl-N-(5-methyl-thiophen-2-ylmethyl)-benzenesulfonamide

https://huagongshe.com/reaction/254436

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant(2,2-Dimethyloxy-ethyl)-(5-methyl-thiophen-2-ylmethyl)-amineHCID 14788182—
SolventEthyl AcetateHCID 8857—
ProductN-(2,2-Dimethoxy-ethyl)4-methyl-N-(5-methyl-thiophen-2-ylmethyl)-benzenesulfonamideHCID 66859761—

Reaction Conditions

Temperature0 °C

Reaction Steps

Crude (2,2-dimethyloxy-ethyl)-(5-methyl-thiophen-2-ylmethyl)-amine (1) (43.41 g ˜75% pure, 0.15 mol) was dissolved in EtOAc (150 mL) resulting in a yellow solution. Triethylamine (22 mL, 0.16 mol) was added. The mixture was cooled to 0° C. in ice bath. p-Toluenesulfonyl chloride (29.68 g, 0.16 mol) was added in small portions keeping the temperature below 15° C. After addition was complete the mixture was left in ice bath and allowed to slowly warm to room temperature and stirred for 20 hrs. The milky-yellow mixture was diluted with EtOAc (300 mL) and washed with water (2×400 mL), 1 M HCl (2×400 mL), water (1×400 mL), sat NaHCO3 (1×400 mL), and brine (1×400 mL), dried (MgSO4) and condensed to provide the title compound as a reddish-yellow liquid, 50.56 g. Product was not purified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875627B2
Source datasetuspto-grants-2011_01
ORD IDord-9ee59b2efec0401d99b822c76a4adfbf
Source noteuspto-grants-2011_01