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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 557182Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktDiethyl cyanophosphonateHCID 76257—
Edukt1-Benzothiophene-7-carbaldehydeHCID 10702138—
EduktLithium cyanide tetrahydrofuranHCID 86597616—
EduktHCID 178506586HCID 178506586—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzo[b]thiophene-7-acetonitrileHCID 11446611—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08058425B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-0915d12a70bb4f9c900e53642c249424
Quellennotizuspto-grants-2011_11