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HRID 1010552作成日:2026年10月25日

4-Methyloxybenzyl chloride → 1-(4-Methoxy-benzyl)-cyclopropanecarbonitrile

https://huagongshe.com/reaction/1010552

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methyloxybenzyl chlorideHCID 69993—
反応物CyclopropanecarbonitrileHCID 79637—
反応物1-(4-methoxy-benzyl)-cyclopropanecarbonitrile Sodium bis(trimethylsilyl)amideHCID 86603547—
溶媒TetrahydrofuranHCID 8028—
生成物1-(4-Methoxy-benzyl)-cyclopropanecarbonitrileHCID 57456950—

反応手順

1-(4-Methoxy-benzyl)-cyclopropanecarbonitrile Sodium bis(trimethylsilyl)amide (2 M in tetrahydrofuran, 37.5 mL, 75.0 mmol) was slowly added to a solution of cyclopropanecarbonitrile (3.35 g, 49.9 mmol) in THF (30 mL) at room temperature. The reaction mixture was stirred for 20 minutes and then a solution 1-chloromethyl-4-methoxy-benzene (7.83 g, 50.0 mmol) in THF was added. The mixture was heated at reflux for 3 hours and then quenched with a saturated aqueous solution of ammonium chloride (50 mL). The separated aqueous layer was extracted three times with ethyl acetate (50 mL). The combined organic layers were washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride, dried over sodium sulfate, filtered, and evaporated to dryness to give crude 1-(4-methoxy-benzyl)-cyclopropanecarbonitrile, which was used directly in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07977322B2
出典データセットuspto-grants-2011_07
ORD IDord-1bd8c24905204990a787022d4ce7456d
出典メモuspto-grants-2011_07