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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2075191Erstellt: 25. Oktober 2026

Diethyl Ether → Benzofuran-5-yl(phenyl)methanol

https://huagongshe.com/reaction/2075191

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
Edukt1-Benzofuran-5-carbaldehydeHCID 2773875—
EduktHCID 178418255HCID 178418255—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzofuran-5-yl(phenyl)methanolHCID 58415371—

Reaktionsschritte

To a solution of 1-benzofuran-5-carbaldehyde (2.70 g, 18.5 mmol) in 50 mL THF under N2 was added phenylmagnesium bromide 3.0M solution in diethyl ether (7.39 mL, 22.2 mmol). The reaction was allowed to stir for 1 h, then was quenched with NH4Cl sat'd aq., extracted with diethyl ether, washed with brine, dried over anhyd. sodium sulfate, filtered, and concentrated in vacuo to a solid to give benzofuran-5-yl(phenyl)methanol which was used without further purification. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.94 (d, J=2.0 Hz, 1H), δ 7.64 (s, 1H), 7.49 (d, J=8.5 Hz, 1H), 7.36-7.42 (m, 2H), 7.26-7.33 (m, 3H), 7.19 (t, J=7.3 Hz, 1H), 6.92 (d, J=1.5 Hz, 1H), 5.88 (d, J=4.0 Hz, 1H), 5.77-5.83 (m, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07919519B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-2bb8768110694cde84453063495b7b0f
Quellennotizuspto-grants-2011_04