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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394422Generated: November 1, 2026

Sodium Carbonate → 4-(1-Phenyl-1-(3-hydroxymethylphenyl)-methylene)-piperidine-1-carboxylic Acid tert-butyl Ester

https://huagongshe.com/reaction/1394422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant[3-(Hydroxymethyl)phenyl]boronic acidHCID 2734662—
Reactant4-(1-Phenyl-1-iodomethylene)-piperidine-1-carboxylic acid tert-butyl esterHCID 67046555—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(1-Phenyl-1-(3-hydroxymethylphenyl)-methylene)-piperidine-1-carboxylic Acid tert-butyl EsterHCID 6704663271%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 4-(1-iodo-1-phenyl-methylene)-piperidine-1-carboxylic acid tert-butyl ester (0.132 g, 0.33 mmol) and 3-hydroxymethylphenylboronic acid (0.050 g 0.33 mmol) in DME (3 mL) was added 2M sodium carbonate (0.65 mL, 1.30 mmol). The reaction vessel was then flushed with Ar for 10 minutes, Pd2dba3 (0.015 g, 0.016 mmol) was added, the vessel was sealed and the mixture was heated at 90° C. for 16 h. The cooled mixture was filtered (0.45 μm syringe filter) and the filtrate was evaporated. The residue was purified by preparative HPLC to give the title compound (0.037 g, 71%) as a white solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348337B2
Source datasetuspto-grants-2008_03
ORD IDord-d84b80e740eb4bda88f18996c47d246e
Source noteuspto-grants-2008_03