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HRID 1042996作成日:2026年10月25日
3,5-Dimethyl-4-[2-(methyloxy)-5-nitrophenyl]isoxazole → [3-(3,5-Dimethyl-4-isoxazolyl)-4-(methyloxy)phenyl]amine 3-(3,5-dimethyl-4-isoxazolyl)-4-(methyloxy)aniline
https://huagongshe.com/reaction/1042996
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 3,5-Dimethyl-4-[2-(methyloxy)-5-nitrophenyl]isoxazole | HCID 57465570 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | [3-(3,5-Dimethyl-4-isoxazolyl)-4-(methyloxy)phenyl]amine 3-(3,5-dimethyl-4-isoxazolyl)-4-(methyloxy)aniline | HCID 67207803 | — |
反応手順
3,5-Dimethyl-4-[2-(methyloxy)-5-nitrophenyl]isoxazole (for a preparation see Intermediate 61, 68 g, 274 mmol) was dissolved in ethyl acetate (1 l) and the solution washed with sodium sulphite solution (5%, 500 ml). The organic layer was dried (sodium sulphate) and filtered through a 3 cm pad of silica gel. The filtrate was diluted with ethanol (1 l) and added to Pd/C (E101 type NO/W, 10 g) in a 5 l nitrogen/vacuum purged hydrogenation flask under vacuum, The mixture was stirred for 24 h. The mixture was purged with vacuum/nitrogen cycles (×3), filtered through Celite under nitrogen and the filtrate evaporated in vacuo to give [3-(3,5-dimethyl-4-isoxazolyl)-4-(methyloxy)phenyl]amine 3-(3,5-dimethyl-4-isoxazolyl)-4-(methyloxy)aniline (62.3 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08557984B2 |
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| 出典データセット | uspto-grants-2013_10 |
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| ORD ID | ord-ef34c290b3404c5c96cb7ef0fe0f8fad |
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| 出典メモ | uspto-grants-2013_10 |
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