Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277070Generated: November 1, 2026

Triethylamine → (6-Oxopiperidin-2-yl)methyl methanesulfonate

https://huagongshe.com/reaction/2277070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant6-(Hydroxymethyl)piperidin-2-oneHCID 14506313—
SolventDichloromethaneHCID 6344—
Product(6-Oxopiperidin-2-yl)methyl methanesulfonateHCID 90404452—

Reaction Steps

6-(Hydroxymethyl)piperidin-2-one (1.0 g, 7.8 mmol) and Et3N (1.1 ml, 7.8 mmol) in DCM (5 ml) was added into mesyl chloride (0.88 g, 7.8 mmol) in DCM (20 ml) at 0° C. The reaction mixture was stirred at room temperature for 15 mins. The reaction mixture was washed with 1 N HCl (20 ml) and brine (40 ml), dried over anhydrous Na2SO4 and concentrated under reduced pressure to give (6-oxopiperidin-2-yl)methyl methanesulfonate which was used in the next step without additional purification. Yield (quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133154B2
Source datasetuspto-grants-2015_09
ORD IDord-d7b04cd1ce0e4bb3a353ab45b4e6d790
Source noteuspto-grants-2015_09