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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016068Generated: October 31, 2026

Dimethyl Sulfoxide → tert-butyl N-(4-oxocyclohexyl)carbamate

https://huagongshe.com/reaction/1016068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178418329HCID 178418329—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Producttert-butyl N-(4-oxocyclohexyl)carbamateHCID 151253591.7%

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a solution of oxalyl chloride (2.33 mL, 26.7 mmol) in methylene chloride (50 mL) cooled at −60° C. was added a solution of DMSO (4 mL, 56 mmol) in methylene chloride (5 mL) followed by a solution of trans-4-tert-butoxycarbonylaminocyclohexanol (5 g, 23 mmol) obtained above in methylene chloride (20 mL). After stirring at −60° C. for 20 minutes, triethylamine (16.1 mL, 116 mmol) was added. The mixture was allowed to warm to room temperature and stirring was continued for 30 minutes. Water was added. The organic phase was separated and the aqueous layer was extracted with methylene chloride twice. The combined organic phase was washed with brine, dried over MgSO4 and concentrated. Flash chromatography eluting with a gradient of 3% to 5% to 10% MeOH/CH2Cl2 provided 4.5 g (90%) of the title compound. MS (M+H)+ 214. found 236 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985730B2
Source datasetuspto-grants-2011_07
ORD IDord-9f968d2ddae14c579b145a4d20fbfaaf
Source noteuspto-grants-2011_07