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HRID 323292作成日:2026年10月27日

Methyl phenylacetate → Methyl 3-cyano-2-phenylpropanoate

https://huagongshe.com/reaction/323292

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl phenylacetateHCID 7559—
反応物BromoacetonitrileHCID 11534—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 3-cyano-2-phenylpropanoateHCID 18464584—

反応手順

Combine methyl phenylacetate (2.0 g, 13.32 mmol) and tetrahydrofuran (15 mL). Cool in a dry-ice/acetone bath. Add dropwise a solution of lithium diisopropylamide (6.66 mL, 2 M in THF, 13.32 mmol). After 1 hour, add α-bromoacetonitrile (1.6 g, 13.32 mmol). After 2 hours, warm the reaction mixture to ambient temperature and partition the reaction mixture between ethyl acetate and water. Separate the aqueous layer and extract three times with ethyl acetate. Dry the combined organic layers over Na2SO4, filter, and concentrate in vacuo to obtain a residue. Distill the residue bulb-to-bulb to give the title compound: bp; 150° C. at 0.5 mm Hg; Rf=0.72 (silica gel, 25% ethyl acetate/hexane).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211199B1
出典データセットuspto-grants-2001_04
ORD IDord-94c4d080b6c14409865112be5c287e5b
出典メモuspto-grants-2001_04