반응 #366019

ord-48378449b0f54b70b94276432adeb1cb

반응 방정식

O=C1c2ccc(O)cc2C(=O)c2ccc(O)cc21
2,6-Dihydroxyanthraquinone
CCCCC(CC)CBr
2-ethylhexyl bromide
O=C([O-])[O-].[K+].[K+]
K2CO3
CCCCC(CC)COc1ccc2c(c1)C(=O)c1ccc(OCC(CC)CCCC)cc1C2=O
product
수율 128.3%
CCCCC(CC)COc1ccc2c(c1)C(=O)c1ccc(OCC(CC)CCCC)cc1C2=O
2,6-di(2-ethylhexyloxy)anthraquinone
수율 128.3%

용매

반응 조건

온도
90°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Most of DMF was removed
  2. 2
    workup.ADDITION500 mL of water was added
  3. 3
    추출The reaction was extracted with ether (3×400 mL)
  4. 4
    세척washed with brine (1×200 mL)
  5. 5
    건조dried over MgSO4
  6. 6
    기타Solvent was removed
  7. 7
    기타the crude product was recrystallized from methanol

실험 절차

2,6-Dihydroxyanthraquinone (100.0 g, 0.42 mol) and 2-ethylhexyl bromide (165.0 g, 0.86 mol) were dissolved in 1 L of DMF. To this solution was added anhydrous K2CO3 (120.0 g, 0.87 mol). The reaction was heated at 90° C. overnight. Most of DMF was removed and 500 mL of water was added. The reaction was extracted with ether (3×400 mL), washed with brine (1×200 mL), and dried over MgSO4. Solvent was removed and the crude product was recrystallized from methanol to give yellow powdery product 125.2 g (65% yield). 1H NMR (CDCl3) δ(ppm): 0.92-0.98 (m, 12H, CH3), 1.34-1.54 (m, 16H), 1.75-1.81 (m, 2H, CH(CH3)), 4.02 (d, J=5.5 Hz, 4H, OCH2), 7.19 (d, J=8.4 Hz, 2H), 7.70 (s, 2H), 8.19 (d, J=8.5 Hz, 2H); 13C NMR (CDCl3): 11.12, 14.06, 23.04, 23.88, 29.08, 30.51, 39.34, 71.34, 110.64, 120.84, 127.00, 129.62, 135.88, 164.29, 182.27. M.p. 49-51° C.; FD-MS: m/z 464 (M+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06361887B1uspto-grants-2002_03