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HRID 566265作成日:2026年10月25日

Methyl phenylacetate → Methyl 3-cyano-2-phenylpropanoate

https://huagongshe.com/reaction/566265

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 diethylamideHCID 11137085—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 3-cyano-2-phenylpropanoateHCID 18464584—

反応手順

A solution of methyl phenylacetate (200 g, 1.33 mol) in THF (300 mL) is added, dropwise, to a −78° C. solution of lithium diethylamide (LDA, 1.4 mol) in THF (2500 mL). After addition is complete, a precipitate forms, and additional THF (200 mL) is added. The resulting mixture is vigorously stirred while a solution of bromoacetonitrile (168 g, 1.4 mol) in THF (400 mL) is slowly added. After 20 minutes the cooling bath is removed and the reaction mixture is quenched with saturated NH4Cl solution (500 mL). After allowing the mixture to slowly warm to ambient temperature any solid material is removed by filtration and the solvent is removed in vacuo. The residue is dissolved in ET2O (1000 mL) and diluted with H2O (1000 mL). The organic phase is then washed with 0.5N HC1 (1×1000 mL), saturated NaCl solution (2×1000 mL) and concentrated in vacuo. The residue is then vacuum distilled (˜1 mm Hg) and the fraction boiling between 125° C. and 145° C. is collected to give β-(carbomethoxy)-β-phenylpropionitrile which solidifies upon standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06174888B1
出典データセットuspto-grants-2001_01
ORD IDord-e1a6647632854a4c8358485c435b2a24
出典メモuspto-grants-2001_01