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HRID 431694作成日:2026年10月27日

2-(Trimethylsilyl)ethanol → Trimethylsilanylethyl 2-fluoro-4-iodobenzoate

https://huagongshe.com/reaction/431694

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Trimethylsilyl)ethanolHCID 18013—
反応物2-Fluoro-4-iodobenzoic acidHCID 2774516—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物Trimethylsilanylethyl 2-fluoro-4-iodobenzoateHCID 54147505—

反応手順

To a solution of 115.5 mg (0.4 mmol) of 2-fluoro-4-iodobenzoic acid (Compound B) in 10 mL of dichloromethane (under a blanket of argon) was added 91.5 mg (0.5 mmol) of 1-(3-dimethylaminopropyl-3-ethyl carbodiimide hydrochloride) and 53 mg (0.4 mmol) of 4-dimethylaminopyridine. To this reaction mixture was added 0.16 ml (132 mg, 1.1 mmol) of 2-trimethylsilylethanol and the resultant mixture was allowed to stir at ambient temperature for 23 hours. The reaction mixture was extracted between ethyl ether and water and the layers were separated. The aqueous phase was washed with ethyl ether (2×50 mL) and the organic phases were combined. The combined organic phase was washed with brine, dried over MgSO4, filtered and concentrated in vacuo to a clear, colorless oil. Purification by flash chromatography (silica, 3% ethyl acetate in hexane) gave the title compound as a clear, colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660755B2
出典データセットuspto-grants-2003_12
ORD IDord-0c4e45554f2a47ea83143b4db26ef270
出典メモuspto-grants-2003_12