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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624352Generated: October 31, 2026

Dimethyl Sulfoxide → Di-tert-butyl (2-oxopropane-1,3-diyl)dicarbamate

https://huagongshe.com/reaction/1624352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactanttert-butyl N-{3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}carbamateHCID 375632—
ReactantAcetone cardiceHCID 18522661—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductDi-tert-butyl (2-oxopropane-1,3-diyl)dicarbamateHCID 1570432088.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of dimethyl sulfoxide (25.2 ml, 0.36 mol) in methylene chloride (357 ml) at −78° C. (dry ice/acetone) was added a solution of oxalyl chloride (20 ml, 0.23 mol) in methylene chloride (115 ml). The reaction mixture was stirred at −78° C. for 30 min under an atmosphere of N2 then a solution of (3-tert-Butoxycarbonylamino-2-hydroxy-propyl)-carbamic acid tert-butyl ester (31.9 g, 0.11 mol) in methylene chloride (300 ml) and triethylamine (75 ml, 0.54 mol) were added. The reaction was stirred for 16 hours, allowing the reaction to warm up to room temperature. The mixture was diluted with water (800 ml) and extracted with methylene chloride (2×300 ml). The combined organic extracts were dried (Na2SO4), filtered, and concentrated in vacuo to afford a yellowish oil. Purification via column chromatography on silica gel (ethyl acetate:hexane, 3:7, v/v) afforded the product as a white solid (28 g, 88%). 1H NMR (CDCl3) δ 1.44 (s, 18H), 4.04 (m, 4H), 5.19 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778967B2
Source datasetuspto-grants-2014_07
ORD IDord-2a1402df2ace47a6a6fe1b0bce8cf482
Source noteuspto-grants-2014_07