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4-Nitrobenzoyl chloride → Ethanone,2-diazo-(4-nitrophenyl)-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| 反応物 | Diazomethane | HCID 9550 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 1-Methyl-2-nitro-1-nitrosoguanidine | HCID 9562060 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | Ethanone,2-diazo-(4-nitrophenyl)- | HCID 138152 | — |
反応手順
The ethereal diazomethane solution [prepared by adding 12.5 g n-methyl-n-nitro-n-nitroso guanidine to potassium hydroxide (50%, 20 ml) and ether (200 ml) at 0°, stirring for 1 hr, and decanting the ether layer; 65% presumed yield] is treated with TEA (7.7 ml) at 0°, then dropwise with p-nitrobenzoyl chloride (10.21 ml) in ether (25 ml). After stirring for 19 hrs, the reaction is filtered through celite and concentrated to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05220021 |
| 出典データセット | uspto-grants-1993_06 |
| ORD ID | ord-ec9c738cda3543fe863edba5cb923f72 |
| 出典メモ | uspto-grants-1993_06 |