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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1374896생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1374896

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물2-Bromobutanoyl bromideHCID 117293—
반응물5-Amino-5-methylhex-3-yne hydrochlorideHCID 21078427—
용매DichloromethaneHCID 6344—
용매Diethylether hexaneHCID 21584099—
생성물2-bromo-N-(5-methylhex-3-yn-5-yl)butyramideHCID 21078407—

반응 조건

온도5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07166621B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-d7c5bd26e1644a5494df15002bbab2ca
출처 메모uspto-grants-2007_01