Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactantcis-4-(tert-Butoxycarbonylamino)cyclohexanolHCID 1514287—
SolventDichloromethaneHCID 6344—
Producttrans-4-(Boc-amino)cyclohexyl methanesulfonateHCID 2188261358%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296732B2
Source datasetuspto-grants-2016_03
ORD IDord-3d7252a4c91e47449365191a35706324
Source noteuspto-grants-2016_03