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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 380128Erstellt: 24. Oktober 2026

2-Bromo-1,2-diphenylethan-1-one → 2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate

https://huagongshe.com/de/reaction/380128

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-1,2-diphenylethan-1-oneHCID 102630—
EduktSodiumHCID 5360545—
Edukt1-(3-Benzyloxybenzoyl)-2-piperidinecarboxylic acidHCID 18367416—
KatalysatorSulfuric AcidHCID 1118—
LösungsmittelEthanolHCID 702—
Produkt2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylateHCID 5424785628,4%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Sodium (54 mg) was dissolved in ethanol (8.0 ml), and then 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylic acid (665 mg), conc. sulfuric acid (1 drop), and desyl bromide (539 mg) was successively dissolved thereto. The resulting mixture was stirred at 70° C. for 2 days, cooled to room temperature, and partitioned between ethyl acetate and 1N HCl. The organic layer was washed with 1N HCl, aqueous sodium bicarbonate, and brine, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed over silica gel to afford 2-oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate (297 mg) as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06300344B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-969536c747cd4b3a94fb701bec284060
Quellennotizuspto-grants-2001_10