반응 #1256710

ord-fba5f1ca6ddd40c6bf95fc79e14f1bb2

반응 방정식

Cc1cncc(C)c1-c1c(C)cc(OS(=O)(=O)C(F)(F)F)cc1C
triflate
Cc1cncc(C)c1-c1c(C)cc(OS(=O)(=O)C(F)(F)F)cc1C
trifluoromethanesulfonic acid 4-(3,5-dimethyl-pyridin-4-yl)-3,5-dimethyl-phenyl ester
O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
N=C(c1ccccc1)c1ccccc1
benzophenone imine
Cc1cncc(C)c1-c1c(C)cc(N=C(c2ccccc2)c2ccccc2)cc1C
title compound
수율 97.7%
Cc1cncc(C)c1-c1c(C)cc(N=C(c2ccccc2)c2ccccc2)cc1C
4-(3,5-dimethylpyridin-4-yl)-N-(diphenylmethylene)-3,5-dimethyl-benzenamine
수율 97.7%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The tube was evacuated
  2. 2
    기타The Schlenk tube was sealed
  3. 3
    기타the mixture was degassed by three freeze-thaw cycles
  4. 4
    workup.STIRRINGThe mixture was then stirred at 65° C. for 15 h
  5. 5
    workup.ADDITIONdiluted with methylene chloride (40 mL)
  6. 6
    여과filtered
  7. 7
    농축the filtrate was concentrated in vacuo
  8. 8
    기타The resulting yellow solid was purified by flash chromatography on silica gel
  9. 9
    세척eluting with 1:1 hexane

실험 절차

A flame-dried sealable Schlenk tube was charged with triflate 8 (0.359 g, 1.00 mmol), Cs2CO3 (0.456 g, 1.40 mmol), Pd(OAc)2 (6.7 mg, 0.030 mmol), and BINAP (28.2 mg, 0.0450 mmol). The tube was evacuated and then backfilled with N2. Next, a solution of benzophenone imine (0.224 g, 1.20 mmol) in dry THF (4 mL) was added with stirring under an N2 flow. The Schlenk tube was sealed, the mixture was degassed by three freeze-thaw cycles, and backfilled with N2. The mixture was then stirred at 65° C. for 15 h. The reaction mixture was next cooled to room temperature, diluted with methylene chloride (40 mL), filtered, and the filtrate was concentrated in vacuo. The resulting yellow solid was purified by flash chromatography on silica gel, eluting with 1:1 hexane: ethyl acetate, to give 0.381 g (97.7%) of the title compound as a colorless solid: mp 44-45° C.; 1H NMR (400 MHz, CD2Cl2): δ 8.305 (s, 2H), 7.774 (d, 2H, J=8.0 Hz), 7.494-7.408 (m, 3H), 7.271 (m, 3H), 7.144 (d, 2H, J=6.8 Hz), 6.476 (s, 2H), 1.828 (s, 6H), 1.706 (s, 6H); 13C NMR (100 MHz, CD2Cl2): δ 168.647, 151.523, 148.783, 148.611, 140.013, 136.737, 135.099, 132.206, 131.678, 131.114, 130.040, 129.685, 128.912, 128.583, 128.038, 120.459, 19.842, 16.594; MS(ESI): m/z 391.5 [(M+H)+, 100]; Anal. Calcd. for C28H26N2: C, 86.12; H, 6.71; N, 7.17. Found; C, 85.86; H, 6.74; N, 7.17.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07824582B2uspto-grants-2010_11