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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691415Generated: November 2, 2026

Dimethyl Sulfoxide → tert-Butyl N-(3-oxopropyl)carbamate

https://huagongshe.com/reaction/1691415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl N-(3-hydroxypropyl)carbamateHCID 3838134—
SolventDichloromethaneHCID 6344—
Producttert-Butyl N-(3-oxopropyl)carbamateHCID 1091005195.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of (3-hydroxy-propyl)-carbamic acid tert-butyl ester (3.0 g, 0.017 mol), N,N-diisopropylethylamine (7.31 mL, 0.042 mol), and dimethyl sulfoxide (1.84 mL, 0.026 mol) in dichloromethane (100 mL) was cooled to 0° C. and flushed with nitrogen. Sulfur trioxide-pyridine complex (6.68 g, 0.042 mol) was added under a stream of nitrogen and the reaction mixture was stirred for 2.5 h. The reaction mixture was quenched using 0.1 N HCl. The aqueous layer was discarded. The organic extract was washed with additional 0.1N HCl (2×) and brine(2×), dried with Na2SO4, filtered, and concentrated to dryness to provide the title compound (2.8 g) as a clear oil which was used without further purification. 1H NMR (DMSO, 400 mHz) δ (ppm): 9.57 (s, 1H), 6.81 (bs, 1H), 3.19-3.14 (m, 2H), 2.49-2.44 (m, 2H), 1.3 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153686B2
Source datasetuspto-grants-2012_04
ORD IDord-6779ab01eca743e78ac47fd542b54c84
Source noteuspto-grants-2012_04