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Hydrochloric Acid → (E)-N,N-diethyl-1,4-diaminobut-2-ene dihydrochloride

HRID 1449649
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HRID 1449649 반응식
[C:1]1(=O)[N:5]([CH2:6]/[CH:7]=C/CBr)[C:4](=O)[C:3]2=[CH:12][CH:13]=CC=[C:2]12.C([NH:19]CC)C.[F-].[K+].[ClH:24]>C(#N)C.C(O)(=O)C>[ClH:24].[ClH:24].[CH2:1]([N:5]([CH2:6][CH3:7])[CH2:4]/[CH:3]=[CH:12]/[CH2:13][NH2:19])[CH3:2]
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참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 8021DiethylamineHCID 522689Potassium FluorideHCID 105168412-(4-Bromobut-2-en-1-yl)isoindoline-1,3-dione

생성물 1

HCID 23352203(E)-N,N-diethyl-1,4-diaminobut-2-ene dihydrochloride수율 41%

시약·촉매·용매 2

HCID 176Acetic Acid
용매
HCID 6342Acetonitrile용매

실험 절차

(E)-1-Phthalimido-4-bromobut-2-ene (4.2 g, 15 mmol), diethylamine (1.1 g, 15 mmol) and KF supported on Celite (7.5 g) were stirred together in acetonitrile (75 ml) at 40° C. for 18 h. The solution was filtered, and the filtrate was concentrated in vacuo to afford an oil, which was dissolved in glacial acetic acid (30 ml) and conc. HCl (30 ml). The mixture was heated at reflux for 30 h. The solution was cooled, filtered and the solvents were removed in vacuo to afford (E)-N,N-diethyl-1,4-diaminobut-2-ene dihydrochloride as an oil (1.32 g, 41%). δH (90 MHz, D2O) 1.19 (6H, m) 3.24 (4H, q), 4.05 (4H, m) and 5.96 (2H, m).

후처리

  1. filtrationThe solution was filtered
  2. concentrationthe filtrate was concentrated in vacuo
  3. customto afford an oil, which
  4. temperatureThe mixture was heated
  5. temperatureat reflux for 30 h
  6. temperatureThe solution was cooled
  7. filtrationfiltered
  8. customthe solvents were removed in vacuo

출처 및 근거

ORD 기록
ord-7f19bd30dab849c0b8e40129287258e8
출처 데이터셋
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05599847

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