Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42144Generated: October 25, 2026

Trifluoroacetic acid → 4-[2-(4-Methanesulfonylphenoxymethyl)pyridin-5-yl]piperidine

https://huagongshe.com/reaction/42144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-[2-(4-methanesulfonyl-phenoxymethyl)pyridin-5-yl]piperidine-1-carboxylateHCID 44819975—
SolventDichloromethaneHCID 6344—
Product4-[2-(4-Methanesulfonylphenoxymethyl)pyridin-5-yl]piperidineHCID 6708315998.3%

Reaction Steps

To a solution of tert-butyl 4-[2-(4-methanesulfonyl-phenoxymethyl)pyridin-5-yl]piperidine-1-carboxylate (Example 1) (164 mg, 0.367 mmol) in dichloromethane (1.5 mL) was added trifluoroacetic acid (1.5 mL). The mixture was stirred at room temperature overnight and was then concentrated in vacuo. To the residue was added saturated aqueous sodium hydrogen carbonate solution and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound (125 mg, yield 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536176B2
Source datasetuspto-grants-2013_09
ORD IDord-7bbf671fa1444f3896c4b029c89881db
Source noteuspto-grants-2013_09