참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Potassium Bromide | HCID 253877 | — |
| 반응물 | 5-[4-(Trifluoromethyl)phenyl]-1,3,4-oxadiazol-2-amine | HCID 5216085 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 3-Ethoxy-5-[4-(trifluoromethyl)phenyl]-4H-1,2,4-triazole | HCID 178467488 | — |
반응 단계
5-[4-(Trifluoromethyl)phenyl]1,3,4-oxadiazol-2-amine (10 g, 44 mmol) and potassium hydroxide (7.4 g, 0.132 mol) dissoved in abs. ethanol (300 ml) were heated at reflux for 3 h. After being cooled to 24° C., the solution was neutralized with acetic acid and concentrated by rotary evaporation. The residue was taken up in ethyl acetate and washed with water and brine. Recrystallization from acetonitrile/ether (2:1) gave 9 g (82%); mp 151-152° C.; IR(KBr, υ=cm-1) 2996, 1534, 1460, 1330, 1162, 1130, 1070; 1H NMR (300 MHz, DMSO-d6) δ 1.35 (3H, t, J=7.1 Hz), 4.38 (2H, q, J=7.0 Hz), 7.82 (2H, d, J=8.3 Hz), 8.10 (2H, d, J=8.1 Hz), 13.64 (1H, br. s); MS(DCl)m/z: 258 (MH+)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06077861 |
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| 출처 데이터셋 | uspto-grants-2000_06 |
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| ORD ID | ord-69af224711d946e2834e454383a0c8a0 |
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| 출처 메모 | uspto-grants-2000_06 |
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