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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776559Generated: October 31, 2026

1,2-Dichloroethane → 2-(Benzyloxy)-2-oxoethyl 4-(methylsulfonamido-methyl)benzoate

https://huagongshe.com/reaction/1776559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantBenzyl 2-hydroxyacetateHCID 561337—
Reactant4-{[(Methylsulfonyl)amino]methyl}benzoic acidHCID 1506609—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventDichloromethane methanolHCID 21226129—
Product2-(Benzyloxy)-2-oxoethyl 4-(methylsulfonamido-methyl)benzoateHCID 8667951560.7%

Reaction Steps

To a solution of 4-(methylsulfonamidomethyl)benzoic acid (0.4 g, 1.745 mmol) and benzyl 2-hydroxyacetate (0.290 g, 1.745 mmol) in a mixture of DCM and THF 1/1 (50 ml), EDC (0.334 g, 1.745 mmol) and DMAP (0.256 g, 2.094 mmol) were added in one portion. The reaction was stirred at RT for 3 hours. The solvent was removed under vacuum and the resulting crude was portioned between EtOAc and HCl 2N. The organic phase was separated, washed with brine and dried over Na2SO4. The solvent was removed under vacuum affording 2-(benzyloxy)-2-oxoethyl 4-(methylsulfonamido-methyl)benzoate (0.4 g, 1.060 mmol, 60.7% yield, MS/ESI+ 377.9 [MH]+). This product was employed in the following step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265768B2
Source datasetuspto-grants-2016_02
ORD IDord-ac348c8047d345f4a89be2d61033404a
Source noteuspto-grants-2016_02