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Undecane → 4-(2-fluorobenzyloxy)-N-methyl-N-methoxybenzamide

HRID 410001
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HRID 410001 반응식
[F:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[CH2:4][O:5][C:6]1[CH:14]=[CH:13][C:9]([C:10]([OH:12])=O)=[CH:8][CH:7]=1.CCCCCCCCCCC.Cl.[CH3:31][O:32][NH:33][CH3:34]>S(Cl)(Cl)=O.C(Cl)Cl>[F:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[CH2:4][O:5][C:6]1[CH:7]=[CH:8][C:9]([C:10]([N:33]([CH3:34])[O:32][CH3:31])=[O:12])=[CH:13][CH:14]=1
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참가 물질

6

반응물 3

HCID 14257UndecaneHCID 81138Methanamine, N-methoxy-, hydrochloride (1:1)HCID 64628464-[(2-Fluorobenzyl)oxy]benzoic acid

생성물 1

HCID 866704624-(2-fluorobenzyloxy)-N-methyl-N-methoxybenzamide수율 93%

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 24386
Thionyl Chloride
용매

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온도
65 °C

실험 절차

4-(2-fluorobenzyloxy)benzoic acid (P2, 5.5 g, 22.3 mmol) was suspended in thionyl chloride (16.5 mL) and heated to 65° C. and held for 3 hours during which time the reactor was kept under a slow sweep of nitrogen. The mixture was then concentrated to a thick oil under hi vac to remove all traces of residual thionyl chloride. The residue was then diluted in CH2Cl2 (20 mL) and cooled to 0° C. In a separate flask, a solution of diaza(1,3)bicycle[5.4.0]undecane (DBU, 8.0 mL, 8.15 g, 53.52 mmol) and N-methoxy-N-methyl amine hydrochloride (2.61 g, 26.76 mmol) in CH2Cl2 (20 mL) was made and slowly added to the solution at 0° C. After warming to 20-25° C., the mixture was washed with 1 M HCl and then with a saturated NaHCO3 solution. After drying over Na2SO4, the solution was concentrated to a thick residue. The mixture was then purified by flash column chromatography eluting with 0→100% EtOAc/hexanes (gradient). Concentration of the fractions containing the title compound gave an oil that crystallized upon standing (6.0 g, 93% yield).

후처리

  1. concentrationThe mixture was then concentrated to a thick oil under hi vac
  2. customto remove all traces of residual thionyl chloride
  3. additionThe residue was then diluted in CH2Cl2 (20 mL)
  4. temperaturecooled to 0° C
  5. additionslowly added to the solution at 0° C
  6. temperatureAfter warming to 20-25° C.
  7. washthe mixture was washed with 1 M HCl
  8. dry with materialAfter drying over Na2SO4
  9. concentrationthe solution was concentrated to a thick residue
  10. customThe mixture was then purified by flash column chromatography
  11. washeluting with 0→100% EtOAc/hexanes (gradient)
  12. additionConcentration of the fractions containing the title compound
  13. customgave an oil that
  14. customcrystallized

출처 및 근거

ORD 기록
ord-29c3bad77b8746d7b506312e0a248605
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08759542B2

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