Formic Acid → Trismethoxyresveratrol

HRID 1411222

반응식

HRID 1411222 반응식
C(N(CC)CC)C.C(O)=O.[CH3:11][O:12][C:13]1[CH:14]=[C:15](/[CH:29]=[CH:30]/[C:31]2[CH:36]=[CH:35][C:34]([O:37][CH3:38])=[CH:33][CH:32]=2)[CH:16]=[C:17]([O:27][CH3:28])[C:18]=1OS(C(F)(F)F)(=O)=O>CN(C=O)C.CC([O-])=O.CC([O-])=O.[Pd+2].C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.[Fe+2]>[CH3:11][O:12][C:13]1[CH:14]=[C:15](/[CH:29]=[CH:30]/[C:31]2[CH:32]=[CH:33][C:34]([O:37][CH3:38])=[CH:35][CH:36]=2)[CH:16]=[C:17]([O:27][CH3:28])[CH:18]=1

참가 물질

7

반응물 3

HCID 284Formic AcidHCID 8471TriethylamineHCID 71812665trans-3,4',5-Trimethoxy-4-(trifluoromethanesulfonyloxy)stilbene

생성물 1

HCID 5388063Trismethoxyresveratrol

시약·촉매·용매 3

HCID 167845palladium(II) acetate촉매HCID 635956Ferrocene-1,1'-bis-(diphenylphosphine)촉매HCID 6228Dimethylformamide용매2회

실험 절차

To a round-bottomed flask (100 mL) equipped with magnetic stir bar was charged anhydrous DMF (6 mL) and triethylamine (960 mg, 9.5 mmol, 5 equiv). In dropwise fashion, 98% formic acid (437 mg, 9.5 mmol, 5 equiv) was added over 10 min. After allowing the mixture to cool to room temperature, a previously prepared solution of 7 (790 mg, 2 mmol) in anhydrous DMF (3 mL) was added in one portion followed by Pd(OAc)2 (21 mg, 0.09 mmol) and DPPF (105 mg, 0.18 mmol). A reflux condenser was equipped and the reaction mixture was heated under N2 to an internal temperature of 80° C. After 20 min the mixture had become dark and the reaction was complete by TLC analysis. The mixture was cooled to room temperature and partitioned between H2O (50 mL) and Et2O (50 mL). A rag layer formed and the mixture was filtered through medium filter paper. The organic layer was separated and washed with H2O (50 mL) and then brine (50 mL). After drying over anhydrous MgSO4, evaporation of the organic phase under reduced pressure left a pale brown oil that slowly crystallized (470 mg, 91%), mp. 55-57° C., lit 56-57° C. 1H NMR (CDCl3): δ 7.45 (d, J=8.9 Hz, 2H), 7.05 (d, J=16 Hz, 1H), 6.90 (d, J=16 Hz, 1H), 6.89 (d, J=8.6 Hz, 2H), 6.65 (d, J=2.2 Hz, 2H), 6.38 (t, J=2.5 Hz, 1H), 3.83 (s, 9H); 13C NMR (CDCl3): 161.20, 139.93, 130.16, 128.96, 128.02, 126.81, 114.37, 104.57, 99.86, 55.57, 55.53. Anal. Calcd for C17H18O3: C, 75.53; H, 6.71. Found: C, 75.53; H, 6.62. (E. Späth and K. Kromp, Ber., 74, 189 (1941)).

후처리

  1. customTo a round-bottomed flask (100 mL) equipped with magnetic stir bar
  2. customA reflux condenser was equipped
  3. temperaturethe reaction mixture was heated under N2 to an internal temperature of 80° C
  4. temperatureThe mixture was cooled to room temperature
  5. custompartitioned between H2O (50 mL) and Et2O (50 mL)
  6. customA rag layer formed
  7. filtrationthe mixture was filtered through medium
  8. filtrationfilter paper
  9. customThe organic layer was separated
  10. washwashed with H2O (50 mL)
  11. dry with materialAfter drying over anhydrous MgSO4, evaporation of the organic phase under reduced pressure
  12. waitleft a pale brown oil that
  13. customslowly crystallized (470 mg, 91%), mp. 55-57° C.
  14. customlit 56-57° C

출처 및 근거

ORD 기록
ord-7c0e23dc79c5432cb33f67f0708701df
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08921614B1

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