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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 576133Erstellt: 24. Oktober 2026

Sodium Hydroxide → 2-(3,4-Dichloro-phenyl)-oxirane

https://huagongshe.com/de/reaction/576133

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt2-Bromo-1-(3,4-dichlorophenyl)ethanoneHCID 244751—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
Produkt2-(3,4-Dichloro-phenyl)-oxiraneHCID 1352171450%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 2-bromo-1-(3,4-dichlorophenyl)ethanone (5.1 g, 18.96 mmol) in methanol (50 mL) at 0° C. was added sodium borohydride (2.1 g, 56.98 mmol). The reaction mixture was stirred at 0° C. for 1 hour. The pH was adjusted to 12 using 2 M sodium hydroxide solution, the solvent was then removed under reduced pressure and the residue was dissolved in dichloromethane. The resultant solution was washed with brine, dried over sodium sulfate, and concentrated under reduced pressure to give 2-(3,4-dichlorophenyl)oxirane (1.79 g, 50% crude). The crude product was used in the next step without further purification: 1H NMR (CDCl3, 500 MHz) 7.41 (d, J=8.5 Hz, 1H), 7.36 (d, J=2.0 Hz, 1H), 7.12 (dd, J=8.5, 2.0 Hz, 1H), 3.81 (dd, J=4.0, 2.5 Hz, 1H), 3.14 (dd, J=5.5, 4.0 Hz, 1H), 2.73 (dd, J=5.5, 2.5 Hz, 1H); ESI MS m/z 189 [M]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09034899B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-e055acaff45a429ebc198503ac47097a
Quellennotizuspto-grants-2015_05