반응 #613162

ord-e20de384567c4138967ddc336962212b

반응 방정식

Nc1cccc2c(N)cccc12
Naphthalene-1,5-diamine
CCCCCCCCBr
1-bromooctane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCCCCCCCN(CCCCCCCC)c1cccc2c(N(CCCCCCCC)CCCCCCCC)cccc12
N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine
수율 38.3%

용매

반응 조건

온도
110°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The reaction was quenched with water
  2. 2
    추출extracted with ether three times
  3. 3
    세척The combined organic phase was washed three times with water
  4. 4
    기타evaporated
  5. 5
    기타to give black oil which
  6. 6
    workup.DISTILLATIONwas distilled under reduced pressure at 90° C.
  7. 7
    기타to yield a black tar
  8. 8
    기타This was purified with flash chromatography
  9. 9
    기타to obtain colourless oil which
  10. 10
    기타crystallised

실험 절차

Naphthalene-1,5-diamine (3.14 g, 19.8 mmol), 1-bromooctane (25.25 g, 0.130 mol), potassium carbonate (11.79 g, 85.3 mmol), and potassium iodide (0.05 g, 0.30 mmol) was stirred in dry butanol (150 ml) and heated to 110° C. for 36 h. The reaction was quenched with water and extracted with ether three times. The combined organic phase was washed three times with water and evaporated to give black oil which was distilled under reduced pressure at 90° C. to yield a black tar. This was purified with flash chromatography using hexane as mobile phase to obtain colourless oil which crystallised to yield N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine (2.3 g, 3.79 mmol) as white crystals. 1H-NMR (CDCl3, δ): 0.85 (t, 12H), 1.0-1.4 (m, 40H), 1.4-1.6 (m, 8H), 3.08 (t, 8H), 7.1 (d, 2H), 7.35 (t, 2H), 8.01 (d, 2H) MS MALDI-TOF (m/z): 606.574

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09343198B2uspto-grants-2016_05