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HRID 1374896作成日:2026年10月25日

Water → 2-bromo-N-(5-methylhex-3-yn-5-yl)butyramide

https://huagongshe.com/reaction/1374896

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物2-Bromobutanoyl bromideHCID 117293—
反応物5-Amino-5-methylhex-3-yne hydrochlorideHCID 21078427—
溶媒DichloromethaneHCID 6344—
溶媒Diethylether hexaneHCID 21584099—
生成物2-bromo-N-(5-methylhex-3-yn-5-yl)butyramideHCID 21078407—

反応条件

温度5 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07166621B2
出典データセットuspto-grants-2007_01
ORD IDord-d7c5bd26e1644a5494df15002bbab2ca
出典メモuspto-grants-2007_01