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HRID 217501作成日:2026年10月23日

Diiodomethane → 3-Iodo-5-(trifluoromethyl)benzyl alcohol

https://huagongshe.com/ja/reaction/217501

反応式

関与物質

役割名称HCID仕込み量
反応物DiiodomethaneHCID 6346—
反応物Tert-Butyl nitriteHCID 10906—
反応物(3-Amino-5-(trifluoromethyl)phenyl)methanolHCID 53414333—
生成物3-Iodo-5-(trifluoromethyl)benzyl alcoholHCID 19261572—

反応条件

温度100 °C

反応手順

[3-amino-5-(trifluoromethyl)phenyl]methanol (500 mg, 5.2 mmol) was suspended in CH2I2 (5 mL) and t-butyl nitrite (622 μL, 5.2 mmol) was added dropwise by syringe. The reaction was heated slowly to 100° C. and was maintained at this temperature for 30 minutes. The reaction was then cooled to room temperature, diluted with hexanes (50 mL), loaded on a silica gel column, and purified with 100% hexanes to 25% EtOAc/hexanes to afford [3-iodo-5-(trifluoromethyl)phenyl]methanol. Rf=0.19 (15% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 7.91 (s, 1H), 7.87 (s, 1H), 7.59 (s, 1H), 4.73 (d, J=4.9 Hz, 2H), 1.86 (t, J=5.6 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193365B2
出典データセットuspto-grants-2012_06
ORD IDord-c7e60889980145c685fe43173f581339
出典メモuspto-grants-2012_06