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HRID 1060373作成日:2026年10月25日

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

https://huagongshe.com/reaction/1060373

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Sodium hydrideHCID 24758—
反応物Benzenesulfonic acid, 3-nitro-, (2R)-2-oxiranylmethyl esterHCID 146513—
反応物2-Chloro-6-hydroxybenzonitrileHCID 4407995—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
溶媒HexaneHCID 8058—
生成物(R)-2-chloro-6-(oxiran-2-ylmethoxy)benzonitrileHCID 44186486—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06521667B1
出典データセットuspto-grants-2003_02
ORD IDord-49a3f58f31094250ae2d5679604c4181
出典メモuspto-grants-2003_02