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HRID 50563作成日:2026年10月27日
Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → (2E)-3-(6-Quinolinyl)-2-propenal
https://huagongshe.com/reaction/50563
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 | 6-Quinolinecarbaldehyde | HCID 765653 | — |
| 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-Quinolinyl)-2-propenal | HCID 22630911 | 65% |
反応手順
A mixture of 6-quinolinecarboxaldehyde (1.58 g, 10.05 mmol, prepared as described in U.S. Pat. No. 5,559,256), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (6.45 g, 15.02 mmol), and TDA-1 (3.20 mL, 10.00 mmol) in dichloromethane (50 mL) and sat. aq. K2CO3 (50 mL) was heated to reflux for 5 h. The layers were separated and the aqueous layer was extracted with dichloromethane (2×25 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (MgSO4), and concentrated. THF (25 mL) and 10% HCl (25 mL) were added and the mixture was stirred for 1 h at rt. The reaction mixture was cooled to 0° C., made basic with 10% NaOH, and extracted with ethyl acetate (3×25 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (MgSO4), and concentrated. Chromatography (SiO2, 1:1 hexane/ethyl acetate+0.2% triethylamine) provided a yellow solid that was partitioned between ethyl acetate (20 mL) and 10% HCl (15 mL). The aqueous layer was washed with ethyl acetate (2×20 mL) and then made basic with 10% NaOH. The precipitated solids were collected by filtration, washed with water, and dried in vacuo to give 1.20 g (65%) of the title compound as a light yellow solid. MS 184 (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-75163e7710824cac99facc83330079da |
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| 出典メモ | uspto-grants-2004_03 |
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