関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Bromobutanoyl bromide | HCID 117293 | — |
| 反応物 | 5-Amino-5-methylhex-3-yne hydrochloride | HCID 21078427 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Diethylether hexane | HCID 21584099 | — |
| 生成物 | 2-bromo-N-(5-methylhex-3-yn-5-yl)butyramide | HCID 21078407 | — |
反応手順
5-Amino-5-methylhex-3-yne hydrochloride (2.21 g) was dissolved in dry dichloromethane (50 ml) and cooled to 5° C. with stirring. 2-Bromobutyryl bromide (3.45 g) was added to the mixture and dry triethylamine (4.17 ml) was added dropwise while maintaining the reaction temperature between 8–15° C. by cooling during the addition. The suspension, which had formed during the reaction, was diluted with further dry dichloromethane (20 ml) and stirred at 5° C. for 0.5 hours. The mixture was allowed to warm to ambient temperature and stirred for a further 2 hours. The reaction was treated with water and extracted with dichloromethane. The organic phase was separated, washed with water (three times), dried over magnesium sulphate and evaporated under reduced pressure to give a brown oil. The oil was fractionated by chromatography (silica; hexane/diethyl ether, 1:1 by volume) to give the required product, as a pale yellow solid, 3.17 g, m.p. 53–55° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07166621B2 |
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| 出典データセット | uspto-grants-2007_01 |
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| ORD ID | ord-d7c5bd26e1644a5494df15002bbab2ca |
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| 出典メモ | uspto-grants-2007_01 |
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