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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 178418329 | HCID 178418329 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl N-(4-oxocyclohexyl)carbamate | HCID 1512535 | 98.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05691323 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-5cab01c70cd148a78bef45a4d260ae97 |
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| Source note | uspto-grants-1997_11 |
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