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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246650Generated: October 27, 2026

tert-butyl N-(4-oxocyclohexyl)carbamate → Tert-butyl 4-(tert-butylsulfinylimino)cyclohexylcarbamate

https://huagongshe.com/reaction/246650

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-oxocyclohexyl)carbamateHCID 1512535—
ReactantTert-ButanesulfinamideHCID 3382465—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(tert-butylsulfinylimino)cyclohexylcarbamateHCID 7127965867.2%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of tert-butyl 4-oxocyclohexylcarbamate (1.0 g, 4.7 mmol), 2-methylpropane-2-sulfinamide (0.63 g, 5.17 mmol) and Ti(OEt)4 (2.1 g, 9.2 mmol) in 10 mL of THF was stirred at 50-60° C. overnight. The mixture was cooled to room temperature and the residue purified by column chromatography (silica gel, 200-300 mesh, eluting with a mixture of petroleum ether and ethyl acetate (4:1, v/v) to give tert-butyl 4-(tert-butylsulfinylimino)cyclohexylcarbamate (1.0 g, 67%) as an clear oil. MS: (M+H)+=317.3; 1H NMR (300 MHz, CDCl3): δ 4.88-4.86 (m, 1H), 3.83 (brs, 1H), 3.39-3.38 (m, 1H), 2.62-2.15 (m, 5H), 1.68-1.53 (m, 2H), 1.43 (s, 9H), 1.24 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-adb60c4cd1774ff3ad8097427af5df33
Source noteuspto-grants-2014_02