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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854330Generated: October 30, 2026

Methanesulfonyl chloride → Benzyl 4-fluoro-4-{[(methylsulfonyl)oxy]methyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/854330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzyl 4-fluoro-4-(hydroxymethyl)piperidine-1-carboxylateHCID 22135584—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-fluoro-4-{[(methylsulfonyl)oxy]methyl}piperidine-1-carboxylateHCID 22135556—

Reaction Steps

To a solution of benzyl 4-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate (1.0 g, 3.7 mmol) in CH2Cl2 (10 mL) at RT was added MsCl (0.29 mL, 3.7 mmol) and TEA (1.04 mL, 7.5 mmol). The reaction mixture was stirred at RT for 5 min, and partitioned between EtOAc and H2O. The organic layer was dried over Na2SO4, filtered, concentrated and purified on silica gel (10:1 to 1:2 hexanes:EtOAc) to give benzyl 4-fluoro-4-{[(methylsulfonyl)oxy]methyl}piperidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259157B2
Source datasetuspto-grants-2007_08
ORD IDord-f81ca437702d40e4bf7acb49c8587468
Source noteuspto-grants-2007_08