関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diiodomethane | HCID 6346 | — |
| 反応物 | Tert-Butyl nitrite | HCID 10906 | — |
| 反応物 | (3-Amino-5-(trifluoromethyl)phenyl)methanol | HCID 53414333 | — |
| 生成物 | 3-Iodo-5-(trifluoromethyl)benzyl alcohol | HCID 19261572 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08193365B2 |
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| 出典データセット | uspto-grants-2012_06 |
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| ORD ID | ord-c7e60889980145c685fe43173f581339 |
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| 出典メモ | uspto-grants-2012_06 |
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