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HRID 2075211作成日:2026年10月27日

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

https://huagongshe.com/reaction/2075211

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物TriethylsilaneHCID 12052—
反応物1-(Benzofuran-5-yl)-1-phenylpropan-1-olHCID 58415385—
溶媒DichloromethaneHCID 6344—
生成物5-(1-Phenylpropyl)-benzofuranHCID 58415356—

反応条件

温度0 °C

反応手順

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).

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-4e824007acd8468580566e8c952934a3
出典メモuspto-grants-2011_04