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HRID 50562作成日:2026年10月27日
Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → (2E)-3-(6-Quinoxalinyl)-2-propenal
https://huagongshe.com/reaction/50562
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- | HCID 112414 | — |
| 反応物 | Quinoxaline-6-carboxaldehyde | HCID 763958 | — |
| 反応物 | (1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide | HCID 2724194 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Potassium Carbonate | HCID 11430 | — |
| 生成物 | (2E)-3-(6-Quinoxalinyl)-2-propenal | HCID 22630799 | 65.1% |
反応手順
A mixture of 6-quinoxalinecarboxaldehyde (0.62 g, 3.92 mmol, prepared as described in Photochem. Photobiol. 1991, 54, 7), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (2.50 g, 5.82 mmol), and TDA-1 (1.20 mL, 3.75 mmol) in dichloromethane (20 mL) and sat. aq. K2CO3 (20 mL) was heated to reflux for 4 h. The layers were separated and the aqueous layer was extracted with dichloromethane (2×20 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (Na2SO4), and concentrated. THF (10 mL) and 10% HCl (10 mL) were added and the mixture was stirred for 1 h at rt. The mixture was cooled to 0° C., the precipitated solids were removed by filtration, washed with water and dried in vacuo to give 0.47 g (65%) of the title compound as a tan solid. MS 185 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06713455B2 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-d7424d04e2f24310a1dbd88da33e8436 |
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| 出典メモ | uspto-grants-2004_03 |
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