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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734228Generated: November 2, 2026

Triethylamine → 1,2-Bis(methanesulfonyloxymethyl)cyclohexane, (1R,2R)-

https://huagongshe.com/reaction/1734228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactantrel-(1R,2R)-1,2-CyclohexanedimethanolHCID 11217323—
SolventChloroformHCID 6212—
Product1,2-Bis(methanesulfonyloxymethyl)cyclohexane, (1R,2R)-HCID 25348359.1%

Reaction Steps

To a solution of the compound (2) (71.86 g; 0.499 mol) and triethylamine (151.21 g; 1.497 mol) in chloroform (1 liter), methanesulfonyl chloride (114.27 g; 0.998 mol) is dropwise added under ice-cooling, and the resultant mixture is stirred at room temperature for 6 hours. The reaction mixture is washed with water, dried and concentrated under reduced pressure. Diethyl ether is added to the residue for crystallization, and the precipitated crystals are collected to give trans-1,2-bis(methanesulfonyloxymethyl)cyclohexane (3) (88.57 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532372
Source datasetuspto-grants-1996_07
ORD IDord-4856938a2a674d659e4b023aa0151e8a
Source noteuspto-grants-1996_07