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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243606Generated: November 2, 2026

Dimethyl Sulfoxide → tert-butyl N-methyl-N-(3-oxopropyl)carbamate

https://huagongshe.com/reaction/1243606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMethylamineHCID 6329—
ReactantOxalyl chlorideHCID 65578—
Reactanttert-Butyl (3-hydroxypropyl)methylcarbamateHCID 10375241—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Producttert-butyl N-methyl-N-(3-oxopropyl)carbamateHCID 10442454100.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dimethylsulfoxide (6.22 ml, 87.6 mmol) was dissolved in dry dichloromethane (100 ml) under nitrogen and the solution was cooled to −78° C. with stirring. Oxalyl chloride (3.95 ml, 45.4 mmol) was then added dropwise and the solution was stirred at −78° C. for a further 30 minutes when effervescence had ceased. A solution of 1,1-dimethylethyl (3-hydroxypropyl)methylcarbamate (6.62 g, 35.0 mmol) in dichloromethane (100 ml) was then added dropwise at −78° C. The resultant solution was stirred at −78° C. for 45 minutes, then a solution of methylamine (24.4 ml, 175 mmol) in dichloromethane (50 ml) was added. The resultant solution was allowed to warm to room temperature and stirred for a further 18 h. The reaction mixture was then poured into brine and extracted with dichloromethane three times. The combined organic fractions were then washed with brine, dried (MgSO4) and evaporated. The residue was triturated with diethyl ether and filtered. The solvent was evaporated to give the title compound (6.60 g, 100%) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119109B2
Source datasetuspto-grants-2006_10
ORD IDord-4152c0668aed43b79771701125461947
Source noteuspto-grants-2006_10