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Dimethylformamide → 2,3-Difluoro-5-methoxy-benzoic acid methyl ester

HRID 1527452
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HRID 1527452 반응식
[F:1][C:2]1[C:10]([F:11])=[CH:9][C:8](O)=[CH:7][C:3]=1C(O)=O.[C:13]([O-:16])([O-])=[O:14].[K+].[K+].[CH3:19]I.CN([CH:24]=[O:25])C>CCOC(C)=O>[CH3:19][O:16][C:13](=[O:14])[C:9]1[CH:8]=[C:7]([O:25][CH3:24])[CH:3]=[C:2]([F:1])[C:10]=1[F:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 265967652,3-Difluoro-5-hydroxybenzoic acid

생성물 1

HCID 677985462,3-Difluoro-5-methoxy-benzoic acid methyl ester

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 2,3-difluoro-5-hydroxy-benzoic acid [749230-51-1] (1.00 g, 5.74 mmol; Melford Laboratories Ltd) in DMF (20 mL) was added K2CO3 (1.99 g, 14.4 mmol) and MeI (0.79 mL, 12.6 mmol), followed by stirring at RT overnight. The reaction mixture was diluted with EtOAc, the organics were washed with a saturated aqueous NH4Cl solution (50 mL) and a saturated aqueous NaHCO3 solution, dried (Phase separator) and evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel (c-hexane/EtOAc 3:1) to afford the title compound as a colorless oil. TLC, Rf (c-hexane/EtOAc 3:1)=0.37; MS (LC/MS): 203.0 [M+H]+; tR (HPLC conditions c): 4.72 min.

후처리

  1. washthe organics were washed with a saturated aqueous NH4Cl solution (50 mL)
  2. dry with materiala saturated aqueous NaHCO3 solution, dried (Phase separator)
  3. customevaporated under reduced pressure
  4. customThe residue was purified by flash column chromatography on silica gel (c-hexane/EtOAc 3:1)

출처 및 근거

ORD 기록
ord-e73d457beeb74514bcf216855fb2df92
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085555B2

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