関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 2-Chlorobenzaldehyde | HCID 6996 | — |
| 反応物 | Ethyl 4-(2-azidoethoxy)-3-oxobutanoate | HCID 13663141 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Ethyl (2-Azidoethoxy)aceto-2-(2-chlorophenylmethlene)acetate | HCID 71433737 | 42.5% |
反応手順
A mixture of 4-(2-azido-ethoxy)-3-oxo-butyric acid ethyl ester (3 g, 13.94 mmol), 2-chlorobenzaldehyde (3 g, 21.34 mmol) and pyridine (1.5 mL, 1.47 g, 18.55 mmol) in EtOH (14 mL) was heated to 60° C. and maintained at this temperature for 3 h. The mixture was concentrated in vacuo. The concentrate was taken up in EtOAc (100 mL), washed successively with 1N HCl (25 mL) and brine (25 mL), dried (Na2SO4), filtered, concentrated in vacuo. The crude product was purified by chromatography using the ISCO Combiflash SQ16× (120 gram Redisep silica gel column, 0 to 60% EtOAc in hexanes for 30 min at 40 mL/min) to afford 2.00 g of 2-[2-(2-azido-ethoxy)-acetyl]-3-(2-chloro-phenyl)-acrylic acid ethyl ester (mixture of E/Z isomers) and 1.01 g of recovered starting material.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07166603B2 |
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| 出典データセット | uspto-grants-2007_01 |
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| ORD ID | ord-d761410f56434816b019b794e0c13c65 |
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| 出典メモ | uspto-grants-2007_01 |
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