HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931481Generated: October 25, 2026
Water → trans-4-(Boc-amino)cyclohexyl methanesulfonate
https://huagongshe.com/reaction/931481
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | cis-4-(tert-Butoxycarbonylamino)cyclohexanol | HCID 1514287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | trans-4-(Boc-amino)cyclohexyl methanesulfonate | HCID 21882613 | 58% |
Reaction Steps
To a solution of tert-butyl N-(4-hydroxycyclohexyl)carbamate (3.8 g, 17.65 mmol, 1.00 equiv) and triethylamine (3.9 g, 38.54 mmol, 2.20 equiv) in dichloromethane (40 mL) was added methanesulfonyl chloride (2.43 g, 21.21 mmol, 1.21 equiv) dropwise with stirring at 0° C. The reaction mixture was stirred overnight at room temperature. Water (50 mL) was added to quench the reaction. The resulting mixture was extracted with 3×50 mL of dichloromethane. The combined organic layers was washed with 2×200 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum to give 3.0 g (58%) of tert-butyl N-[4-(methanesulfonyloxy)cyclohexyl]carbamate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09296732B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-3d7252a4c91e47449365191a35706324 |
|---|
| Source note | uspto-grants-2016_03 |
|---|