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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451788Generated: October 25, 2026

Triethylamine → 2-(Benzyloxycarbonylamino)-3-(1-methylcyclohexyl)propyl methanesulfonate

https://huagongshe.com/reaction/451788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzyl 1-hydroxy-3-(1-methylcyclohexyl)propan-2-ylcarbamateHCID 59201634—
SolventDichloromethaneHCID 6344—
Product2-(Benzyloxycarbonylamino)-3-(1-methylcyclohexyl)propyl methanesulfonateHCID 86639448—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 0.3607 g (1.18 mmol) of benzyl 1-hydroxy-3-(1-methylcyclohexyl)propan-2-ylcarbamate, 0.4 mL (2.87 mmol, 2.43 equiv) of triethylamine, 0.1 mL (1.29 mmol, 1.09 equiv) of methanesulfonyl chloride in CH2Cl2 (10 mL) was stirred at 0° C. for 1.5 h. The reaction mixture was quenched with ice water, extracted with CH2Cl2, washed with aqueous NaHCO3, and dried over Na2SO4. After the solvent was removed in vacuo, the crude 2-(benzyloxycarbonylamino)-3-(1-methylcyclohexyl)propyl methanesulfonate was used directly in the next step without further purification. MS ESI +ve m/z 406 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487108B2
Source datasetuspto-grants-2013_07
ORD IDord-955a3d1e77ea42498895707e1b154213
Source noteuspto-grants-2013_07