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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063372Generated: November 1, 2026

Trifluoroacetic acid → 3-Piperidin-4-ylprop-2-ynyl methanesulfonate;2,2,2-trifluoroacetic acid

https://huagongshe.com/reaction/1063372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(3-Methanesulfonyloxy-prop-1-ynyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 86585277—
SolventDichloromethaneHCID 6344—
Product3-Piperidin-4-ylprop-2-ynyl methanesulfonate;2,2,2-trifluoroacetic acidHCID 86585278—

Reaction Steps

A solution of 2.96 g (9.4 mmol) of 4-(3-Methanesulfonyloxy-prop-1-ynyl)-piperidine-1-carboxylic acid tert-butyl ester in 50 ml CH2Cl2 was treated at 0° C. with 25.2 ml of TFA (for 20 min). After 30 min at this temperature, the reaction was evaporated, evaporated again with toluene (4 times) and dried to give 3.6 g (quantitative) of methanesulfonic acid 3-piperidin-4-yl-prop-2-ynyl ester; compound with trifluoro-acetic acid, MS: 218 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964974B2
Source datasetuspto-grants-2005_11
ORD IDord-7e03f128aa5c49228053fc0c3e17dcc5
Source noteuspto-grants-2005_11