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HRID 31162作成日:2026年10月26日

Malononitrile, (1-naphthylmethylene)- → 2-[(2-Methoxyphenyl)(1-naphthyl)methyl]malononitrile

https://huagongshe.com/reaction/31162

反応式

関与物質

役割名称HCID仕込み量
反応物Malononitrile, (1-naphthylmethylene)-HCID 18092—
反応物HCID 178489560HCID 178489560—
溶媒TetrahydrofuranHCID 8028—
生成物2-[(2-Methoxyphenyl)(1-naphthyl)methyl]malononitrileHCID 11716587—

反応手順

A flask was charged with (1-naphthalenylmethylene)-propanedinitrile (408 mg, 2 mmol) and 10 mL anhydrous tetrahydrofuran. To this stirred solution was added, at room temperature, 2-methoxy phenyl magnesium bromide (2.4 mL, 2.4 mmol, 1 M in tetrahydrofuran). The reaction was stirred 1.5 hours, after which it was quenched with 1 N hydrochloric acid and taken up in ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate, brine, dried over magnesium sulfate, filtered, and evaporated to dryness. Following purification on silica (20% ethyl acetate/hexanes) 551 mg product was isolated as an off white foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425580B2
出典データセットuspto-grants-2008_09
ORD IDord-b2ea1113d63c49478e6a3ed96726ce5a
出典メモuspto-grants-2008_09