تفاعل #75451

ord-23461bdad4054a56a320bb8926e582fc

معادلة التفاعل

O=C(c1ccccc1)c1ccc(CBr)cc1
4-Bromomethylbenzophenone
CCN(CCO)c1ccccc1
2-(N-Ethylanilino)ethanol
[H-].[Na+]
NaH
CCN(CCOCc1ccc(C(=O)c2ccccc2)cc1)c1ccccc1
desired product
المردود 80.0%
CCN(CCOCc1ccc(C(=O)c2ccccc2)cc1)c1ccccc1
4-([N-Ethyl-N-phenyl-2-aminoethyl]oxymethyl)benzophenone
المردود 80.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
20°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirring
  2. 2
    workup.WAITcontinued for 72 hours
  3. 3
    أخرىExcess solvent was removed in vacuo
  4. 4
    workup.ADDITIONthe residue diluted with DCM
  5. 5
    غسيلwashed with water and NaHCO3 solution (sat.)
  6. 6
    تجفيفdried (MgSO4) and solvent
  7. 7
    أخرىremoved under vacuum
  8. 8
    أخرىThe resulting oil was purified by flash chromatography
  9. 9
    غسيلeluting with petroleum (bp 40-60° C.)

الإجراء التجريبي

2-(N-Ethylanilino)ethanol (3.03 g, 18.4 mmol, 1.2 eq) in THF (20 cm3) was treated with NaH (60% dispersion in oil, 524 mg, 13,1 mmol, 1.4 eq) and stirred at 20° C. for 1 hour. 4-Bromomethylbenzophenone (4.21 g, 15.3 mmol) was then added and stirring continued for 72 hours. Excess solvent was removed in vacuo and the residue diluted with DCM, washed with water and NaHCO3 solution (sat.), dried (MgSO4) and solvent removed under vacuum. The resulting oil was purified by flash chromatography, eluting with petroleum (bp 40-60° C.):EtOAc (9:1), to give the desired product as a yellow oil (4.36 g, 80%), Rf=0.54 (4:1, petrol:EtOAc) (Found: C, 78.34; H, 6.86; N, 5.29. C24H25NO2 requires C, 80.19; H, 7.01; N, 3.90%); νmax (film/cm−1 1658 (s), 1598 (s), 1506 (s); δH (200 MHz; CDCl3) 1.22 (3H, t, J 7, CH3), 3.49 (2H, q, J 7, CH2CH3), 3.58-3.79 (4H, m, OCH2CH2N), 4.66 (2H, s, ArCH2O), 6.69-6.79 (3H, m, ArH o- and p- to NR2), 7.28 (2H, dd, J 7, 7, ArH m- to NR2), 7.46-7.68 (5H, m, ArH), 7.80-7.88 (4H, m, ArH o- to C═O), δC (50.3 MHz; CDCl3) 12.2 (CH3), 45.5 (NCH2CH3), 50.1 (NCH2CH2O), 68.5 (NCH2CH2O), 72.2 (ArCH2O), 111.8 (ArCH o- to NR2), 115.8 (ArCH p- to NR2), 127.0, 128.3, 129.3, 130.0 and 130.3 (ArCH o- and m- to C═O and ArCH m- to NR2), 132.4 (ArCH p- to C═O), 136.8 and 137.7 (4° ArCC═O), 143.2 (4° ArCCH2O), 147.7 (4° ArCNR2), 196.4 (C═O); m/z (APCI+) 360 ([M+H]+, 30%); HRMS C24H26O2N requires 360.1963; found 360.1963.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06699527B1uspto-grants-2004_03