化工社化工社 化学情報印刷レポート · 研究参考用
5-Bromoisatin → 5-Bromo-3-hydroxy-3-prop-1-ynyl-1,3-dihydroindol-2-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Bromoisatin | HCID 6889 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | HCID 178419101 | HCID 178419101 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-Bromo-3-hydroxy-3-prop-1-ynyl-1,3-dihydroindol-2-one | HCID 12085938 | 97% |
反応手順
To a solution of 5-bromoisatin (2.5 g, 11 mmol) in dry THF (100 cm3) at −10° C. under a nitrogen atmosphere was added 1-propynylmagnesium bromide (0.5 M in THF, 47 cm3, 23.5 mmol). After 1 h, the mixture was poured into saturated ammonium chloride and extracted with EtOAc (×3), washed with brine, dried (MgSO4) and evaporated to afford 5-bromo-3-hydroxy-3-prop-1-ynyl-1,3-dihydroindol-2-one (2.83 g, 10.6 mmol, 97%) which was used without further purification: (CDCl3) δ 1.83 (s, 3H), 6.79 (d, 1H, J=8.0 Hz), 6.90 (s, 1H), 7.41–7.44 (m, 2H), 10.59 (s, 1H); MS ((−) ESI) m/z 264 (M−H)−.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07084168B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-11c8f6a6d49c4e53ba77cc33793f0bd3 |
| 出典メモ | uspto-grants-2006_08 |