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HRID 462147作成日:2026年10月25日
4-(Chloromethyl)-2-nitroanisole → Benzenemethanaminium, N,N-bis[3-(formylamino)propyl]-4-methoxy-N-methyl-3-nitro-, chloride (1:1)
https://huagongshe.com/reaction/462147
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4-(Chloromethyl)-2-nitroanisole | HCID 80785 | — |
| 反応物 | Formamide, N,N'-[(methylimino)di-3,1-propanediyl]bis- | HCID 3084810 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | Benzenemethanaminium, N,N-bis[3-(formylamino)propyl]-4-methoxy-N-methyl-3-nitro-, chloride (1:1) | HCID 100848 | — |
反応手順
A mixture of 54.0 parts of N,N-bis(3-formamidopropyl)methylamine, 50.4 parts of 4-methoxy-3-nitrobenzyl chloride, and 78 parts of acetonitrile was stirred at reflux for seven and a half hours. An additional 78 parts of acetonitrile was added to the reaction mixture causing an oil to separate. Heating at reflux was continued for an additional two hours and the 140 parts of acetonitrile was distilled away and 200 parts of water was added. The remaining acetonitrile was removed by distillation and the cooled reaction mixture was filtered with the aid of diatomaceous earth to obtain an aqueous solution of N-methyl-N-(3-nitro-4-methoxybenzyl)-N,N-bis(3-formamidopropyl)ammonium chloride. The solution was used directly for reduction of the nitro group.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04065500 |
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| 出典データセット | uspto-grants-1977_12 |
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| ORD ID | ord-273833c9c1fc4afeb25732ae8da2b3d8 |
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| 出典メモ | uspto-grants-1977_12 |
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