関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | 4-(1H-Pyrrol-3-ylmethyl)-morpholine | HCID 57587018 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-Morpholin-4-ylmethyl-1H-pyrrole-2-carbaldehyde | HCID 86650824 | — |
反応手順
To a solution of DMF (66 mmoles) in DCM there is added, dropwise, at 0° C., POCl3. After stirring for 5 minutes, a solution of the compound obtained in Step B (33 mmoles) in DCM (60 ml) is added dropwise. After stirring for 4 hours at 0° C. and for 30 minutes at reflux, an aqueous solution of sodium acetate (110 mmoles) is added. After a further 30 minutes at reflux, aqueous 2M sodium hydroxide solution is added at ambient temperature until the pH is alkaline (9-10). The solution is stirred for 2 hours at ambient temperature, and then 300 ml of DCM are added. After extracting with DCM, the organic phase is washed with water and with saturated aqueous NaCl solution, dried over sodium sulphate, filtered and evaporated to dryness. The residue obtained is purified by flash chromatography on silica gel (SiO2; gradient DCM/AcOEt) to yield the title product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08541412B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-a27ccf32082843b3abb7f8f29a8680ab |
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| 出典メモ | uspto-grants-2013_09 |
|---|