化工社化工社 化学情報印刷レポート · 研究参考用
methyl 3-(4-nitrophenyl)-1H-pyrrole-2-carboxylate → methyl 3-(4-aminophenyl)-1H-pyrrole-2-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | methyl 3-(4-nitrophenyl)-1H-pyrrole-2-carboxylate | HCID 18616331 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | methyl 3-(4-aminophenyl)-1H-pyrrole-2-carboxylate | HCID 57756905 | 76.3% |
反応手順
To a suspension of 0.1 g (0.942 mmol) of 10% palladium-on-charcoal in 35 cm3 of methanol is added, at a temperature in the region of 20° C., 1 g (4.061 mmol) of methyl 3-(4-nitrophenyl)-1H-pyrrole-2-carboxylate. After hydrogenating for 20 hours in an autoclave under 3 bar of hydrogen, at a temperature in the region of 35° C., the reaction mixture is filtered, the catalyst is rinsed with twice 5 cm3 of methanol and the filtrate is then concentrated to dryness under reduced pressure (2.7 kPa) to give 0.67 g of methyl 3-(4-aminophenyl)-1H-pyrrole-2-carboxylate in the form of an orange-coloured solid; M.W.=216, IE: m/z=216 M+, m/z=184 [M-CH3OH]+, m/z=155 [M−H2COOCH3]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07560571B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-c67f36321ae247e397c4b81902690b58 |
| 出典メモ | uspto-grants-2009_07 |