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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951213Generated: October 29, 2026

Dimethyl Sulfoxide → Benzyl [2-(2-oxobutylcarbamoyl)ethyl]carbamate

https://huagongshe.com/reaction/1951213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantBenzyl [2-(2-hydroxybutylcarbamoyl)ethyl]carbamateHCID 57637120—
SolventDichloromethaneHCID 6344—
ProductBenzyl [2-(2-oxobutylcarbamoyl)ethyl]carbamateHCID 57637089—

Reaction Steps

To a stirred solution of oxalyl chloride (2 M in DCM) (13.35 ml, 26.5 mmol) in dry DCM at −78° C. is added dropwise DMSO (2.5 ml, 35.4 mmol). After stirring for 15 minutes, the reaction mixture is treated with a solution of [2-(2-hydroxy-butylcarbamoyl)-ethyl]-carbamic acid benzyl ester (step 1) (6.5 g, 22.1 mol) in dry DCM (40 ml). Triethylamine (13 ml) is added after 1 hour and after stirring at −78° C. for 90 minutes, the reaction mixture is allowed to warm to room temperature. The reaction is diluted with DCM (100 ml) and washed with HCl (1M, 200 ml), saturated sodium bicarbonate solution (200 ml), water (200 ml) and brine (200 ml). The organic portion is dried over MgSO4, filtered and concentrated in vacuo to yield the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404684B2
Source datasetuspto-grants-2013_03
ORD IDord-261b6998026f41909e4931c5cc509ae2
Source noteuspto-grants-2013_03