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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713459Generated: October 27, 2026

4-(3-Chloro-4-methoxy-benzoyl)-piperidine-1-carboxylic acid tert-butylester → (3-Chloro-4-methoxy-phenyl)-piperidin-4-yl-methanone

https://huagongshe.com/reaction/713459

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Chloro-4-methoxy-benzoyl)-piperidine-1-carboxylic acid tert-butylesterHCID 71236078—
SolventHydrochloric AcidHCID 313—
Product(3-Chloro-4-methoxy-phenyl)-piperidin-4-yl-methanoneHCID 4313092890.3%

Reaction Steps

To a solution of 4-(3-chloro-4-methoxy-benzoyl)-piperidine-1-carboxylic acid tert-butylester (1.1 g, 3.1 mmol) in 20 mL of 6N HCl, the reaction mixture was stirred at ambient temperature for 18 hours, then solvent was removed by reduced pressure to yield the title product (0.75 g, 2.8 mmol). MS (ESI) m/z 254.0 (M+H+); HPLC (Novapak 150×3.9 mm C-18 column: mobile phase: 35-90% acetonitrile/water with 0.1% TFA, at 2 mL/min over 2 min.) t 1.39 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181266B2
Source datasetuspto-grants-2015_11
ORD IDord-bbc6884f33bc44b49f118a12cef36732
Source noteuspto-grants-2015_11