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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227369Generated: October 25, 2026

Triethylamine → (1-Methylpiperidin-2-yl)methyl methanesulfonate

https://huagongshe.com/reaction/227369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-Methyl-2-piperidinemethanolHCID 89394—
SolventTetrahydrofuranHCID 8028—
Product(1-Methylpiperidin-2-yl)methyl methanesulfonateHCID 44627021—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-methyl-2-piperidine-methanol (Aldrich, 0.27 mL, 2.1 mmol) in 10 mL tetrahydrofuran (THF) at 0° C. was added triethylamine (0.87 mL, 6.22 mmol) followed by methanesulfonyl chloride (0.24 mL, 3.1 mmol). The mixture was stirred at 0° C. for 10 min then the ice-bath was removed and the reaction mixture was stirred at 23° C. for an additional 1.5 h. The reaction mixture was filtered though Celite with THF and concentrated under reduced pressure. This crude material was used directly in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560481B2
Source datasetuspto-grants-2009_07
ORD IDord-a17f828435f94eff96c61b543cf3d75e
Source noteuspto-grants-2009_07