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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1910519Erstellt: 25. Oktober 2026

Dimethylformamide → 1,2-Diphenylethyl 1-methylpiperidine-4-carboxylate

https://huagongshe.com/reaction/1910519

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktOxalyl chlorideHCID 65578—
Edukt1,2-DiphenylethanolHCID 94178—
Edukt4-Piperidinecarboxylic acid, 1-methyl-, hydrochloride (1:1)HCID 2760043—
LösungsmittelDichloromethaneHCID 6344—
Produkt1,2-Diphenylethyl 1-methylpiperidine-4-carboxylateHCID 7092578737%

Reaktionsschritte

Oxalyl dichloride (141 μl, 1.67 mmol) was added dropwise to a solution of 1-methylpiperidine-4-carboxylic acid hydrochloride (300 mg, 1.67 mmol) in DCM (20 ml) and few drops of DMF (catalytic amount). The reaction was stirred at room temperature for 2 hours. The volatiles were removed under vacuum, and the crude was taken up with pyridine (20 ml). 1,2-Diphenylethanol (331 mg, 1.67 mmol) was added, and the resulting suspension was heated under microwave irradiation at 140° C. for 1 hour. Pyridine was removed under vacuum, and the crude was purified by flash chromatography (DCM/MeOH=97/3 to 94/6) to obtain 1,2-diphenylethyl 1-methylpiperidine-4-carboxylate (200 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08604015B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-b13f5ebe1c75469c810a0348eb917fd9
Quellennotizuspto-grants-2013_12