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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713458Generated: October 25, 2026

3-Chloro-4-methoxybenzeneboronic acid → 4-(3-Chloro-4-methoxy-benzoyl)-piperidine-1-carboxylic acid tert-butylester

https://huagongshe.com/reaction/713458

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-methoxybenzeneboronic acidHCID 3247522—
Reactant4-Phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl esterHCID 89375800—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystCuprous 2-thiophenecarboxylateHCID 11194830—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Chloro-4-methoxy-benzoyl)-piperidine-1-carboxylic acid tert-butylesterHCID 7123607888.4%

Reaction Steps

To a mixture of 3-chloro-4-methoxyphenylboronic acid (0.87 g, 4.67 mmol), ligand TFP (0.14 g, 0.6 mmol), Pd2dba3 (0.29 g, 0.31 mmol), copper (I) thiophene-2-carboxylate (0.89 g, 4.7 mmol) was added a solution of 4-phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl ester (1.0 g, 3.1 mmol) in 10 mL of THF while purging with N2 at 50° C. After 18 hours the reaction mixture was diluted with ethyl acetate, filtered through celite then concentrated in vacuo. Purification by flash chromatography gave the title compound (1.02 g, 2.74 mmol). MS (ESI) m/z 354.0 (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 1.42 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181266B2
Source datasetuspto-grants-2015_11
ORD IDord-f5519f890ff84bf9bf6ab184dfd0df64
Source noteuspto-grants-2015_11