Water → 4,4-Dimethyl-1-n-butyl-2-undecyl-2-imidazoline

HRID 2352208

반응식

HRID 2352208 반응식
[CH2:1]([Li])[CH2:2][CH2:3][CH3:4].[CH3:6][C:7]1([CH3:23])[CH2:11][NH:10][C:9]([CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])=[N:8]1.BrCCCC.O>CCCCCC.C1C=CC=CC=1>[CH3:6][C:7]1([CH3:23])[CH2:11][N:10]([CH2:1][CH2:2][CH2:3][CH3:4])[C:9]([CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])=[N:8]1

참가 물질

7

실험 절차

22 ml (55 mmoles) of a 2.5M solution of butyl lithium in hexane are added to 12.62g (50 mmoles) of 4,4-dimethyl-2-undecyl-2-imidazoline in 50 ml of anhydrous benzene at a temperature kept at around 20° C. The mixture is then stirred for 2 hours at ambient temperature (15° to 20° C.). 8.22 g (60 mmoles) of 1 -bromobutane is then added dropwise to the reaction mixture, keeping the temperature at around 20° C. The reaction mixture is then stirred at ambient temperature until it is homogeneous, after which it is refluxed for 3 hours. After cooling, 50 ml of water is added, the mixture is stirred for half hour, decanted and extracted with 100 ml of ether. After drying over magnesium sulfate the solvent is removed in vacuo and the oil is distilled at reduced pressure to give 10.34 g (67%) of the product.

후처리

  1. customkept at around 20° C
  2. customat around 20° C
  3. stirringThe reaction mixture is then stirred at ambient temperature until it
  4. temperatureafter which it is refluxed for 3 hours
  5. temperatureAfter cooling
  6. stirringthe mixture is stirred for half hour
  7. customdecanted
  8. extractionextracted with 100 ml of ether
  9. dry with materialAfter drying over magnesium sulfate the solvent
  10. customis removed in vacuo
  11. distillationthe oil is distilled at reduced pressure

출처 및 근거

ORD 기록
ord-ac3ad2ecf40a4184a46131587ded5c24
출처 데이터셋
uspto-grants-1989_10
특허 번호
US04876249

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