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HRID 465612作成日:2026年10月25日

Bromoacetonitrile → 7-Cyano-5-oxoheptanoic acid

https://huagongshe.com/reaction/465612

反応式

関与物質

役割名称HCID仕込み量
反応物BromoacetonitrileHCID 11534—
反応物4-Acetylbutyric acidHCID 18407—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
溶媒TetrahydrofuranHCID 8028—
生成物7-Cyano-5-oxoheptanoic acidHCID 14986712—

反応手順

To a solution of potassium hexamethyldisilazide (66 ml, 60 mmol) in dry tetrahydrofuran (140 ml) at -70° is added slowly 5-oxohexanoic acid (36 ml, 30 mmol). The resulting yellow suspension is stirred at -70° for 1 h and bromoacetonitrile (2.2 ml, 32 mmol) is added slowly. The reaction mixture is stirred at -70° for 1 h and then at room temperature for 0.5 h. The reaction is quenched by addition of 1N aqueous hydrochloric acid (100 ml). The aqueous layer is extracted twice with ether. Combined organic layer is dried, filtered and evaporated to obtain a dark oil which is purified by silica gel chromatography using 9:1 ether/hexane with 1% acetic acid as eluent to give 7-cyano-5-oxoheptanoic acid as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05153214
出典データセットuspto-grants-1992_10
ORD IDord-8b89643d0bdd44568e4cd81cca446028
出典メモuspto-grants-1992_10