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4-Nitro-1H-indole → Methyl (4-nitro-1H-indol-3-yl)(oxo)acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Nitro-1H-indole | HCID 145766 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | Diphosphoryl tetrachloride | HCID 4432411 | — |
| 反応物 | Methyl oxo-pyrrolidin-1-yl-acetate | HCID 10975749 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Methyl (4-nitro-1H-indol-3-yl)(oxo)acetate | HCID 10243717 | — |
反応手順
9.4 mL (68 mmol) diphosphoryl chloride were slowly added dropwise to 10 g (62 mmol) 4-nitroindole and 11 g (68 mmol) methyl oxo-pyrrolidin-1-yl-acetate with stirring and while cooling with ice. The reaction mixture was heated to RT and stirred for 3 h at RT. Then first of all 10 mL MeOH were added dropwise at 0° C. and then saturated sodium hydrogen carbonate solution was added dropwise at 0° C. After repeated extraction with DCM the organic phase was dried and evaporated down to 100 mL. This residue was left to stand at RT and the precipitate formed was suction filtered, washed and dried in the air.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08829006B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-68e5f506e7274640bd5fd8e1e106861a |
| 出典メモ | uspto-grants-2014_09 |