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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972559Generated: November 2, 2026

Methanesulfonyl chloride → ((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonate

https://huagongshe.com/reaction/1972559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant[(2R)-1,4-dibenzylpiperazin-2-yl]methanolHCID 9994741—
SolventDichloromethaneHCID 6344—
Product((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonateHCID 8667039787.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of (R)-(1,4-dibenzylpiperazin-2-yl)methanol (4.00 g, 13.49 mmol, US2007/0088039) and Hünig's base (2.35 mL, 13.49 mmol) in CH2Cl2 (27 mL) was stirred at 0° C. and methanesulfonyl chloride (1.04 mL, 13.49 mmol) was added drop-wise. The reaction mixture was filtered through a short pad of silica gel, using 19:1 CH2Cl2/Et2O (1000 mL) to rinse. The filtrate was concentrated in vacuo while maintaining the temperature below 25° C. Diethyl ether was added to the residue, the resulting slurry was placed in a sonicator for 1 min, filtered through a fitted funnel and the filtrate was concentrated to give a white solid ((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonate (4.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-c712bca14f8a45769e83740a3d07432c
Source noteuspto-grants-2013_04