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Benzoyl chloride → Diazomethane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzoyl chloride | HCID 7412 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1-Methyl-2-nitro-1-nitrosoguanidine | HCID 9562060 | — |
| 生成物 | Diazomethane | HCID 9550 | — |
| 生成物 | Diazoacetophenone | HCID 18667 | — |
反応手順
An ethereal solution of diazomethane is prepared from n-methyl-n-nitro-n-nitroso guanidine (15.72 g) for an estimated yield of 64 mmol. To the ethereal solution (400 ml) at 0° is added triethylamine (9.0 ml, 64 mmol), then dropwise benzoyl chloride (7.4 ml, 64 mmol). The reaction is warmed to 22° and stirred for 20 hrs, then filtered through celite and concentrated. The residue is recrystallized from ether/pentane 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-7538c669ae334f6eaba262652748a676 |
| 出典メモ | uspto-grants-1993_06 |