関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Iodine | HCID 807 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Phosphorus pentachloride | HCID 24819 | — |
| 反応物 | Ethyl 2-oxo-1-azacyclodecane-10-carboxylate | HCID 19930826 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | cis Ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylate | HCID 131718120 | — |
反応手順
Ethyl 2-oxo-1-azacyclodecane-10-carboxylate (4.0 g, 17.6 mmol) is dissolved in methylene chloride (50 mL), and cooled to 0° C. Phosphorus pentachloride (3.85 g, 18.5 mmol) and iodine (0.051 g, 0.2 mmol) are added. The reaction is stirred for 15 minutes at 0° C. Then, bromine (3.10 g, 19.4 mmol) is added, and the reaction is stirred at 0° C. for 4 hours. The reaction is quenched by adding saturated sodium sulfite (until the color of excess bromine disappears), and extracted several times with methylene chloride. The combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (15% ethyl acetate/hexane) to give cis ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylate, m.p. 132°-134° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05426103 |
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| 出典データセット | uspto-grants-1995_06 |
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| ORD ID | ord-ae6e3feffc3748f18ceeb2c6741450df |
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| 出典メモ | uspto-grants-1995_06 |
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