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
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-butyl N-(4-oxocyclohexyl)carbamate | HCID 1512535 | — |
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-(tert-butylsulfinylimino)cyclohexylcarbamate | HCID 71279658 | 67.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658646B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-adb60c4cd1774ff3ad8097427af5df33 |
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| Source note | uspto-grants-2014_02 |
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