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HRID 2302175생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/2302175

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Sodium hydrideHCID 24758—
반응물Benzenesulfonic acid, 3-nitro-, (2R)-2-oxiranylmethyl esterHCID 146513—
반응물2-Chloro-6-hydroxybenzonitrileHCID 4407995—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
용매HexaneHCID 8058—
생성물(R)-2-chloro-6-(oxiran-2-ylmethoxy)benzonitrileHCID 44186486—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06432656B1
출처 데이터셋uspto-grants-2002_08
ORD IDord-aa37df42a62c413bb4bf456c9464022b
출처 메모uspto-grants-2002_08