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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 713458Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/713458

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Chloro-4-methoxybenzeneboronic acidHCID 3247522—
Edukt4-Phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl esterHCID 89375800—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
KatalysatorCuprous 2-thiophenecarboxylateHCID 11194830—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(3-Chloro-4-methoxy-benzoyl)-piperidine-1-carboxylic acid tert-butylesterHCID 7123607888,4%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181266B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-f5519f890ff84bf9bf6ab184dfd0df64
Quellennotizuspto-grants-2015_11