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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 222464Erstellt: 25. Oktober 2026

Imidazole → 6-(Tert-butyl-diphenyl-silanyloxy)-benzofuran-3-one

https://huagongshe.com/reaction/222464

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
Edukttert-ButyldiphenylchlorosilaneHCID 94078—
Edukt6-Hydroxy-3-coumaranoneHCID 235717—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt6-(Tert-butyl-diphenyl-silanyloxy)-benzofuran-3-oneHCID 68526161—

Reaktionsschritte

To a solution of 6-hydroxy-benzofuran-3-one (1.01 g, 6.73 mmol) in dry dichloromethane (18 mL) was added imidazole (0.458 g, 6.727 mmol) followed by tert-butyldiphenylchlorosilane (1.72 mL, 6.73 mmol) at room temperature. The mixture was stirred overnight and poured into brine. The aqueous phase was extracted with dichloromethane. The combined organic layers were dried over Na2SO4, evaporated in vacuo and the residue was purified by column chromatography (ethylacetate:hexane; 1:9) to give the 6-(tert-butyl-diphenyl-silanyloxy)-benzofuran-3-one as slightly yellow oil (1.34 g, 52%). 1H NMR (CDCl3, 400 MHz) 1.21 (s, 9H), 4.54 (s, 2H), 6.40 (s, 1H), 6.55 (dd, J=1.6, 8.0 Hz, 1H), 7.38-7.50 (m, 7H), 7.67 (m, 4H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08207216B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-6079800153794aac983a1ae9d9c44a76
Quellennotizuspto-grants-2012_06