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Cesium carbonate → HCID 66756714, 화합물

HRID 1642631
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HRID 1642631 반응식
C(O[C:4](=O)[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[C:8]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:7]=1)C.[CH2:24]([O:31][C:32]1[CH:39]=[CH:38][CH:37]=C(F)[C:33]=1[C:34]#[N:35])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.C([O-])([O-])=O.[Cs+].[Cs+]>CN(C=O)C.CCOC(C)=O>[CH2:24]([O:31][C:32]1[CH:39]=[CH:38][CH:37]=[C:4]([CH2:5][C:6]2[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[C:8]([O:15][CH2:16][C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH:7]=2)[C:33]=1[C:34]#[N:35])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1
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6

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HCID 10796Cesium carbonateHCID 30234822-Benzyloxy-6-fluorobenzonitrileHCID 66757012HCID 66757012, 화합물

생성물 1

HCID 66756714HCID 66756714, 화합물

시약·촉매·용매 2

HCID 6228Dimethylformamide용매2회HCID 8857Ethyl Acetate용매

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온도
80 °C

실험 절차

(3-Benzyloxy-4-nitrophenyl)-acetic acid ethyl ester (Step C) (1.90 g, 6.03 mmol) and 2-benzyloxy-6-fluorobenzonitrile (Step D) (2.74 g, 12.1 mmol) are dissolved in DMF (18 mL) and added dropwise to a suspension of Cs2CO3 (5.89 g, 18.1 mmol) in DMF (18 mL). The mixture is heated to 80° C. for 1.5 h, then stirred at 60° C. for 16 h. The mixture is diluted with EtOAc (350 mL) and extracted with 1N HCl (2×75 mL), followed by brine (75 mL). The organic phase is dried over Na2SO4 and concentrated. The residue is taken up in THF (18 mL), MeOH (18 mL) and 1N NaOH (36 mL). Decarboxylation is complete after 2 h, the reaction mixture is poured into ice water (100 mL) and acidified to pH ˜2 with 6N HCl. The mixture is extracted with EtOAc (2×200 mL) and the organic phase is washed with brine (75 mL), dried over Na2SO4 and concentrated to afford a brown oil. Purification by flash column (10-75% EtOAc/hexanes) affords 2-benzyloxy-6-(3-benzyloxy-4-nitrobenzyl)-benzonitrile as an off-white solid: MS (M+H)+=451.

후처리

  1. extractionextracted with 1N HCl (2×75 mL)
  2. dry with materialThe organic phase is dried over Na2SO4
  3. concentrationconcentrated
  4. waitDecarboxylation is complete after 2 h
  5. additionthe reaction mixture is poured into ice water (100 mL)
  6. extractionThe mixture is extracted with EtOAc (2×200 mL)
  7. washthe organic phase is washed with brine (75 mL)
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated
  10. customto afford a brown oil
  11. customPurification by flash column (10-75% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-00bf8f5ff598478faba2a154eb9d0b80
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08119666B2

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