Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602129Erstellt: 24. Oktober 2026

Potassium Bromide → Benzyl 3-formylpiperidine-1-carboxylate

https://huagongshe.com/de/reaction/602129

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium BromideHCID 253877—
EduktSodium BicarbonateHCID 516892—
EduktBenzyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2776577—
EduktSodium HypochloriteHCID 23665760—
KatalysatorTempoHCID 2724126—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzyl 3-formylpiperidine-1-carboxylateHCID 989965390%

Reaktionsschritte

An aqueous solution (2 mL) of potassium bromide (983 mg, 8.26 mmol) was added to 1-benzyloxycarbonyl-3-piperidinyl methanol (2.00 g, 8.02 mmol) and 2,2,6,6-tetramethyl piperidine-N-oxyl (12.5 mg, 0.0802 mmol) in dichloromethane (20 mL). The mixture was stirred for 5 min while chilled in an ice bath. A 0.35 mol/L aqueous sodium hypochlorite solution (25.2 mL, 8.82 mmol) and sodium bicarbonate (1.96 g, 23.3 mmol) were added and the mixture was stirred for 10 min. Subsequently, the reaction mixture was extracted with ethyl acetate and the extract washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the residue by silica gel column chromatography (hexane:ethyl acetate=10:1->2:1) gave 1.78 g (90%) of the desired compound as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902367B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-6e270006b9de40f4a66816fc7ecc256c
Quellennotizuspto-grants-2011_03