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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291196Generated: October 30, 2026

Triethylamine → 1-Benzoylpiperidin-4-ylmethyl methanesulfonate

https://huagongshe.com/reaction/1291196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Piperidinemethanol, 1-benzoyl-HCID 10262870—
SolventDichloromethaneHCID 6344—
Product1-Benzoylpiperidin-4-ylmethyl methanesulfonateHCID 9994786100.3%

Reaction Steps

7.5 g (0.0342 mol) of 1-benzoyl-4-hydroxymethyl-piperidine were dissolved in 170 ml of dichlormethane and 17 ml (0.122 mol) of triethylamine, cooled to 0° and treated with a solution of 3.14 ml (0.0404 mol) of methanesulfonyl chloride in 20 ml of dichloromethane. The mixture was stirred at 0° for 1/2 hr. Then, 100 ml of 1N aqueous HCI were added, the mixture was stirred for 5 min., the organic phase was washed with 1N aqueous HCI, with saturated bicarbonate solution and with saturated sodium chloride solution and dried over sodium sulfate. 10.2 g (100%) of 1-benzoylpiperidin-4-ylmethyl methanesulfonate were obtained as yellow crystals; m.p. 87°-90°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-ebcf76c1ed5f4339bb4bae6e7d47707b
Source noteuspto-grants-1998_05