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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505867Generated: November 3, 2026

Triethylamine → Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/505867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 2765838—

Reaction Steps

A solution of 10.08 g (46.81 mmol) of 1,1-dimethylethyl 4-(hydroxymethyl)piperidine-1-carboxylate and 9.90 ml (70.21 mmol) of triethylamine in 100 ml of dichloromethane, cooled to approximately 0° C., is admixed dropwise under an inert atmosphere with a solution of 4 ml (51.49 mmol) of mesyl chloride in 10 ml of dichloromethane. The bath is removed and stirring is continued at ambient temperature for 30 minutes. Water is added to the reaction mixture, the aqueous phase is separated off and extracted once with dichloromethane, the combined organic phases are washed with water and dried over sodium sulphate and the filtrate is concentrated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781590B2
Source datasetuspto-grants-2010_08
ORD IDord-f7426a8427a1489fb89f66c88f4c03c0
Source noteuspto-grants-2010_08