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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294923Generated: October 31, 2026

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

https://huagongshe.com/reaction/2294923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178418329HCID 178418329—
SolventDichloromethaneHCID 6344—
Producttert-butyl N-(4-oxocyclohexyl)carbamateHCID 151253598.6%

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a stirred solution of oxalyl chloride (0.83 g) in dry dichloromethane (15 mL) at -60° C. was added dimethylsulfoxide (1.0 mL) in dichloromethane (3 mL) dropwise. The reaction mixture was stirred at -60° C. for 10 min, then N-tert-butyloxycarbonyl-trans-4-aminocyclohexanol (1.28 g) in dichloromethane (70 mL) was added over 15 min. The resulting mixture was stirred at -60° C. for a further 15 min, then triethylamine (4.2 mL) was added and the solution was allowed to warm to room temperature. The mixture was washed with water (20 mL) and this aqueous layer was extracted once with dichloromethane (20 mL). The combined organic extracts were dried over MgSO4 and concentrated under reduced pressure. Drying under vacuum gave N-tert-butyloxycarbonyl-4-aminocyclohexanone (1.25 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691323
Source datasetuspto-grants-1997_11
ORD IDord-5cab01c70cd148a78bef45a4d260ae97
Source noteuspto-grants-1997_11