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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842353Generated: November 2, 2026

tert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate → 4-(2-(Trifluoromethyl)phenoxy)piperidine hydrochloride

https://huagongshe.com/reaction/1842353

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 5237175—
Reactant3-(2-Chloro-5-trifluoromethyl-phenoxymethyl)-pyrrolidine hydrochlorideHCID 68088462—
Product4-(2-(Trifluoromethyl)phenoxy)piperidine hydrochlorideHCID 1717800472%

Reaction Steps

The synthesis of intermediate 1n is performed starting with 3-hydroxymethyl-1-BOC-pyrrolidine following the operating mode described for the synthesis of 1a (white solid, total yield 72%). TLC silica gel 60 F 254 Merck, CH2Cl2-MeOH—AcOH: 90:9:1, Rf=0.10

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946225B2
Source datasetuspto-grants-2015_02
ORD IDord-232bf9856edc4ab4a9fda85329a47854
Source noteuspto-grants-2015_02