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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2075211Erstellt: 25. Oktober 2026

Trifluoroacetic acid → 5-(1-Phenylpropyl)-benzofuran

https://huagongshe.com/reaction/2075211

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktTriethylsilaneHCID 12052—
Edukt1-(Benzofuran-5-yl)-1-phenylpropan-1-olHCID 58415385—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(1-Phenylpropyl)-benzofuranHCID 58415356—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of 1-(benzofuran-5-yl)-1-phenylpropan-1-ol (3.14 g, 12.4 mmol) and triethylsilane (2.39 mL, 14.9 mmol) in DCM (10 mL) under nitrogen at 0° C. was added trifluoroacetic acid (4.62 mL, 62.2 mmol) dropwise via syringe. The reaction mixture was stirred at 0° C. for 3 h. Additional triethylsilane (2.39 mL, 14.9 mmol) followed by trifluoroacetic acid (4.62 mL, 62.2 mmol) were added via syringe, and the reaction was brought to room temperature and stirred for 2 h. The reaction mixture was quenched with 1M aqueous NaOH. DCM was added, and the aqueous layer was separated and extracted again with DCM. The combined organic layers were dried (MgSO4) and concentrated to give a crude oil. The crude product was purified by silica flash chromatography to give 5-(1-phenylpropyl)-benzofuran as a transparent oil. MS (ESI) m/z: Calculated: 236.1; Observed: 237.2 (M++1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07919519B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-4e824007acd8468580566e8c952934a3
Quellennotizuspto-grants-2011_04