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HRID 2075191作成日:2026年10月27日

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

https://huagongshe.com/reaction/2075191

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物1-Benzofuran-5-carbaldehydeHCID 2773875—
反応物HCID 178418255HCID 178418255—
溶媒TetrahydrofuranHCID 8028—
生成物Benzofuran-5-yl(phenyl)methanolHCID 58415371—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07919519B2
出典データセットuspto-grants-2011_04
ORD IDord-2bb8768110694cde84453063495b7b0f
出典メモuspto-grants-2011_04