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4-tert-Butylcatechol → Methyl 3-(2-Nitroethyl)-1H-indole-4-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-tert-Butylcatechol | HCID 7381 | — |
| 反応物 | methyl 1H-indole-4-carboxylate | HCID 2733668 | — |
| 反応物 | 2-nitroethyl Acetate | HCID 11815399 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | Methyl 3-(2-Nitroethyl)-1H-indole-4-carboxylate | HCID 14916518 | 79% |
反応手順
A solution of methyl 1H-indole-4-carboxylate (7.34 g, 41.9 mmol), 2-nitroethyl acetate (6.90 g, 51.9 mmol) and 4-tert-butylcatechol (0.026 g, 0.16 mmol) in xylene (50 mL) was refluxed for 6 hrs. The solvent was evaporated under reduced pressure to give a residual dark oily raw product that was purified by short column chromatography on silica using ethyl acetate-light petroleum as eluent. The product was obtained as yellowish solid material in 79% yield. Mp: 103° C. MS m/z 249 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08138333B2 |
| 出典データセット | uspto-grants-2012_03 |
| ORD ID | ord-93ef735e238a42029df9e1e8c9a22d52 |
| 出典メモ | uspto-grants-2012_03 |