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

HRID 1374896

반응식

HRID 1374896 반응식
Cl.[NH2:2][C:3]([CH3:9])([CH3:8])[C:4]#[C:5][CH2:6][CH3:7].[Br:10][CH:11]([CH2:15][CH3:16])[C:12](Br)=[O:13].C(N(CC)CC)C.O>ClCCl.CCCCCC.C(OCC)C>[Br:10][CH:11]([CH2:15][CH3:16])[C:12]([NH:2][C:3]([CH3:9])([CH3:8])[C:4]#[C:5][CH2:6][CH3:7])=[O:13]

참가 물질

7

반응 조건

온도
5 °C

실험 절차

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.

후처리

  1. additionwas added dropwise
  2. temperaturewhile maintaining the reaction temperature between 8–15° C.
  3. temperatureby cooling during the addition
  4. customThe suspension, which had formed during the reaction
  5. stirringstirred at 5° C. for 0.5 hours
  6. temperatureto warm to ambient temperature
  7. stirringstirred for a further 2 hours
  8. extractionextracted with dichloromethane
  9. customThe organic phase was separated
  10. washwashed with water (three times)
  11. dry with materialdried over magnesium sulphate
  12. customevaporated under reduced pressure
  13. customto give a brown oil

출처 및 근거

ORD 기록
ord-d7c5bd26e1644a5494df15002bbab2ca
출처 데이터셋
uspto-grants-2007_01
특허 번호
US07166621B2

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