戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 557182作成日:2026年10月26日

tert-Butanol → Benzo[b]thiophene-7-acetonitrile

https://huagongshe.com/reaction/557182

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物Diethyl cyanophosphonateHCID 76257—
反応物1-Benzothiophene-7-carbaldehydeHCID 10702138—
反応物Lithium cyanide tetrahydrofuranHCID 86597616—
反応物HCID 178506586HCID 178506586—
溶媒TetrahydrofuranHCID 8028—
生成物Benzo[b]thiophene-7-acetonitrileHCID 11446611—

反応手順

Add Benzo[b]thiophene-7-carboxaldehyde (2.34 g, 14.4 mmol) and lithium cyanide tetrahydrofuran complex (LiCN*1.5 Tetrahydrofuran, 204 mg, 1.44 mmol) to tetrahydrofuran (40 mL) under nitrogen. Add dropwise neat diethyl cyanophosphonate (2.8 mL, 18.4 mmol) to the stirring reaction mixture. Stir at room temp under nitrogen for 60 hours. Add 2-methyl-2-propanol (1.4 mL, 14.6 mmol). Add the reaction mixture via cannula to a stirred 0.1 molar solution of samarium(II) iodide in tetrahydrofuran (360 mL, 36.0 mmol) at 25° C. under nitrogen. If the resulting reaction mixture is not deep blue add additional samarium(II) iodide solution until deep blue color persists. Stir the reaction at 25° C. for 1 hour. Concentrate under reduced pressure, dilute with ethyl acetate, diethyl ether (1:1), wash with aqueous 0.1 M hydrochloric acid, and aqueous saturated sodium chloride. Dry the organic phase over anhydrous magnesium sulfate, filter, and concentrate under reduced pressure. Chromatograph on flash silica using a gradient from neat hexane to 25% ethyl acetate in hexane to obtain the title compound as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08058425B2
出典データセットuspto-grants-2011_11
ORD IDord-0915d12a70bb4f9c900e53642c249424
出典メモuspto-grants-2011_11