関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pyrrolidine | HCID 31268 | — |
| 反応物 | 6-Chloro-1,3-dihydroindol-2-one | HCID 736344 | — |
| 反応物 | 5-Chloro-2-(3-hydroxy-propoxy)-benzaldehyde | HCID 57565935 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Z-6-chloro-3-[5-chloro-2-(3-hydroxy-propoxy)-benzylidene]-1,3-dihydro-indol-2-one | HCID 86760828 | 87.6% |
反応手順
5-Chloro-2-(3-hydroxy-1-propoxy)-benzaldehyde (8 g, 37 mmol) and 6-chlorooxindole (6.2 g, 37 mmol) were mixed in anhydrous methanol (20 mL). Then pyrrolidine (3 mL, 37 mmol) was added slowly at r.t. The mixture was heated to 70° C. for 3 h and cooled to room temperature. The precipitate was collected by filtration to give title compound as a yellow solid (Yield: 11.8 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07495007B2 |
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| 出典データセット | uspto-grants-2009_02 |
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| ORD ID | ord-438e668c95e447499ba8cdc223373e7b |
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| 出典メモ | uspto-grants-2009_02 |
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