참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | N-Iodosuccinimide | HCID 120273 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 반응물 | 4-Amino-2-(trifluoromethyl)benzonitrile | HCID 522170 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Aluminum | HCID 5359268 | — |
| 생성물 | 4-Amino-5-iodo-2-(trifluoromethyl)benzonitrile | HCID 25067377 | — |
반응 단계
4-Amino-2-trifluoromethyl-benzonitrile (20.44 g, 109.79 mmoles) and p-toluenesulfonic acid monohydrate (1.05 g, 5.52 mmoles) were dissolved methanol (200 mL) and THF (200 mL), and the reaction mixture was stirred under a nitrogen atmosphere. The reaction vessel was wrapped in aluminium foil, while the solution was stirred for 20 min., then N-iodosuccinimide (30.41 g, 135.17 mmoles) was added and the reaction was allowed to stir overnight (16 hrs). The reaction mixture was concentrated in vacuo, triturated with hexanes (3×400 mL) and concentrated to dryness. The crude solid was dissolved in diethyl ether (400 mL), washed with water (3×), the organic extracts were diluted with hexanes (400 mL) and a white solid precipitated. The solid was filtered and dried in a vacuum oven (35° C. @ 762 Torr) overnight to yield the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434688B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-1a95de0f49494be9891b705ba09698b7 |
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| 출처 메모 | uspto-grants-2016_09 |
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