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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1060373Erstellt: 27. Oktober 2026

Sodium Hydroxide → (R)-2-chloro-6-(oxiran-2-ylmethoxy)benzonitrile

https://huagongshe.com/reaction/1060373

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktSodium hydrideHCID 24758—
EduktBenzenesulfonic acid, 3-nitro-, (2R)-2-oxiranylmethyl esterHCID 146513—
Edukt2-Chloro-6-hydroxybenzonitrileHCID 4407995—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelHexaneHCID 8058—
Produkt(R)-2-chloro-6-(oxiran-2-ylmethoxy)benzonitrileHCID 44186486—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

3-Chloro-2-cyanophenol (0.55 g, 3.58 mmol) was dissolved in 10 mL of dimethylformamide, and the solution cooled to 0° C. Sodium hydride (0.158 g, 3.94 mmol 60% in oil), washed with hexane and dimethylformamide, was added to cooled solution over a period of one minute. After stirring for 10 minutes at room temperature, (2R)-(−)-glycidyl 3-nitrobenzenesulfonate was added and stirred 16 hours. The reaction was poured into ether and dilute sodium hydroxide. The ether layer was separated and the aqueous layer extracted once more with ether. The combined ether extracts were washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give 0.7 g of (R)-3-chloro-2-cyanophenyl glycidyl ether.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06521667B1
Quelldatensatzuspto-grants-2003_02
ORD IDord-49a3f58f31094250ae2d5679604c4181
Quellennotizuspto-grants-2003_02