참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diiodomethane | HCID 6346 | — |
| 반응물 | Tert-Butyl nitrite | HCID 10906 | — |
| 반응물 | (3-Amino-5-(trifluoromethyl)phenyl)methanol | HCID 53414333 | — |
| 생성물 | 3-Iodo-5-(trifluoromethyl)benzyl alcohol | HCID 19261572 | — |
반응 단계
[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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737295B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-bcdbf29868c8476a87c9bbdc191742e7 |
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| 출처 메모 | uspto-grants-2010_06 |
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