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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 557182생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/557182

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물Diethyl cyanophosphonateHCID 76257—
반응물1-Benzothiophene-7-carbaldehydeHCID 10702138—
반응물Lithium cyanide tetrahydrofuranHCID 86597616—
반응물HCID 178506586HCID 178506586—
용매TetrahydrofuranHCID 8028—
생성물Benzo[b]thiophene-7-acetonitrileHCID 11446611—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08058425B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-0915d12a70bb4f9c900e53642c249424
출처 메모uspto-grants-2011_11