Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5477Generated: October 24, 2026

Triethylamine → 1-(Methylsulfonyl)piperidin-4-yl methanesulfonate

https://huagongshe.com/en/reaction/5477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantPiperidin-4-olHCID 79341—
SolventDichloromethaneHCID 6344—
Product1-(Methylsulfonyl)piperidin-4-yl methanesulfonateHCID 2227306589%

Reaction Steps

To a solution of 4-hydroxypiperidine (5.10 g, 50 mmoles) and triethylamine (20.9 ml, 150 mmoles) in methylene chloride (150 ml) was added methanesulfonyl chloride (8.54 ml, 110 mmoles) with stirring under ice-cooling and the mixture was stirred at room temperature for 1 hour. The reaction mixture was washed in turn with an aqueous saturated sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was solidified with ethyl acetate-n-hexane to obtain 11.45 g of the desired product (88.3%, pale yellow solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244908
Source datasetuspto-grants-1993_09
ORD IDord-000317cc53274835920257e50a875bf5
Source noteuspto-grants-1993_09