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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386759Generated: October 31, 2026

4-(3-(2,4-Difluorophenyl)propyl)-1-t-butoxycarbonyl piperidine → 4-(3-(2,4-Difluorophenyl)propyl)piperidine

https://huagongshe.com/reaction/1386759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-(2,4-Difluorophenyl)propyl)-1-t-butoxycarbonyl piperidineHCID 21180776—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product4-(3-(2,4-Difluorophenyl)propyl)piperidineHCID 21180653108.3%

Reaction Steps

A solution of 4-(3-(2,4-difluorophenyl)propyl)-1-t-butoxycarbonylpiperidine (90 mg, 0.27 mmol, from EXAMPLE 113, Step E) in 2 mL of 1% HCl in MeOH was heated to 50° C. for 2 h. After cooling to rt, the material was concentrated to provide 70 mg (93%) of the title compound: HPLC (YMC ODS-A 4.6×50 mm column, gradient elution using 10:90 v/v CH3CN/H2O+0.1% TFA to 100% CH3CN+0.1% TFA over 2.0 min, hold 1 min, 5.0 mL/min, 220 nm): Retention Time: 1.18 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265434B1
Source datasetuspto-grants-2001_07
ORD IDord-e2fb9ea4d12e484cb8db95e0a08395f4
Source noteuspto-grants-2001_07