Citric Acid → 2-(benzamido)-4-((E)-2-(3-methoxyphenyl)vinyl)benzoic acid

HRID 1673388노트

반응식

HRID 1673388 반응식
I[C:2]1[CH:3]=[C:4]([O:8][CH3:9])[CH:5]=[CH:6][CH:7]=1.C(=O)([O-])[O-].[Cs+].[Cs+].[C:16]([NH:24][C:25]1[CH:37]=[C:36]([CH:38]=[CH2:39])[CH:35]=[CH:34][C:26]=1[C:27]([O:29]C(C)(C)C)=[O:28])(=[O:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C(OCC)(=O)C.C1(C)C=CC=CC=1>[C:16]([NH:24][C:25]1[CH:37]=[C:36](/[CH:38]=[CH:39]/[C:2]2[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH3:9])[CH:3]=2)[CH:35]=[CH:34][C:26]=1[C:27]([OH:29])=[O:28])(=[O:23])[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

참가 물질

8

반응물 4

HCID 311Citric AcidHCID 10796Cesium carbonateHCID 69839Benzene, 1-iodo-3-methoxy-HCID 67343635Tert-butyl 2-(benzamido)-4-vinylbenzoate

생성물 1

HCID 578794242-(benzamido)-4-((E)-2-(3-methoxyphenyl)vinyl)benzoic acid

시약·촉매·용매 3

HCID 74236Tetrabutylammonium Bromide촉매HCID 1140Toluene용매HCID 8857Ethyl Acetate용매

반응 조건

온도
110 °C

실험 절차

0.060 mL of 3-iodoanisole, 0.16 g of cesium carbonate, 24 mg of tetrabutylammonium bromide and 39 mg of polymer supported di(acetato)dicyclohexylphosphino palladium(II) were added to 2.0 mL of toluene solution containing 80 mg of tert-butyl 2-(benzamido)-4-vinylbenzoate at room temperature and stirred at 110° C. for 24 hours. After the reaction mixture was cooled to room temperature, ethyl acetate and 10% citric acid aqueous solution were added. The organic layer was separated, and the solvent was evaporated under reduced pressure after washed with 10% citric acid aqueous solution. 10 mL of trifluoroacetic acid was added to the obtained residue and stirred at room temperature for 1 hour. The solvent was evaporated under reduced pressure and the obtained residue was purified with reversed-phase silica gel column chromatography [eluent; 60-100% acetonitrile/0.1% trifluoroacetic acid aqueous solution] to obtain 2-(benzamido)-4-((E)-2-(3-methoxyphenyl)vinyl)benzoic acid.

후처리

  1. temperatureAfter the reaction mixture was cooled to room temperature
  2. customThe organic layer was separated
  3. customthe solvent was evaporated under reduced pressure
  4. washafter washed with 10% citric acid aqueous solution
  5. addition10 mL of trifluoroacetic acid was added to the obtained residue
  6. stirringstirred at room temperature for 1 hour
  7. customThe solvent was evaporated under reduced pressure
  8. customthe obtained residue was purified with reversed-phase silica gel column chromatography [eluent; 60-100% acetonitrile/0.1% trifluoroacetic acid aqueous solution]

출처 및 근거

ORD 기록
ord-3bf06e390471457a8bf4fcd2f236bd49
출처 데이터셋
uspto-grants-2011_08
특허 번호
US07999132B2

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