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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15729Erstellt: 23. Oktober 2026

Ammonium Hydroxide → Benzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylate

https://huagongshe.com/de/reaction/15729

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium HydroxideHCID 14923—
EduktAmmonium ChlorideHCID 25517—
EduktBenzyl 3,4-dihydro-4-oxo-pyridine-1(2H)-carboxylateHCID 11368235—
EduktHCID 178478191HCID 178478191—
EduktHCID 178494437HCID 178494437—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktBenzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylateHCID 59342393—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

CuBr.SMe2 complex (1.49 g, 7.26 mmol) was added to 25 mL of anhydrous THF and cooled to −78° C. 4-Chlorophenylmagnesium bromide (7.26 mL, 1.0 M in THF, 7.26 mmol) was added slowly via syringe. Stirring at −78° C. for 1 hour produced an orange then green-like suspension. Boron trifluoride dimethyl etherate (0.92 mL, 7.26 mmol) was added and stirred for 5 minutes. To the newly formed complex was then added over 1 hour a solution of the compound 66 (1.0 g, 4.32 mmol) in 15 mL of anhydrous THF. After stirring 2 hours at −78° C., 16 mL of aq. 20% NH4Cl/conc. NH4OH (1:1) was added, and the mixture was allowed to warm-up to room temperature. EtOAc was used to extract (3×100 mL) and the combined organic layers were washed with brine and dried (MgSO4). Solvent was removed by rotary evaporation and the residue was purified by flash chromatography to give the product 67 as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732609B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-ab71bfae619241b3a6352d150f024773
Quellennotizuspto-grants-2010_06