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Potassium Carbonate → 2-(4-Fluoro-3-methyl-phenoxy)-hexanoic acid methyl ester

HRID 1361049
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HRID 1361049 반응식
[CH3:1][O:2][C:3](=[O:10])[CH:4](Br)[CH2:5][CH2:6][CH2:7][CH3:8].[F:11][C:12]1[CH:17]=[CH:16][C:15]([OH:18])=[CH:14][C:13]=1[CH3:19].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C.O>[CH3:1][O:2][C:3](=[O:10])[CH:4]([O:18][C:15]1[CH:16]=[CH:17][C:12]([F:11])=[C:13]([CH3:19])[CH:14]=1)[CH2:5][CH2:6][CH2:7][CH3:8]
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참가 물질

6

반응물 3

HCID 11430Potassium CarbonateHCID 95578Hexanoic acid, 2-bromo-, methyl esterHCID 27373944-Fluoro-3-methylphenol

생성물 1

HCID 597751852-(4-Fluoro-3-methyl-phenoxy)-hexanoic acid methyl ester수율 76.4%

시약·촉매·용매 2

HCID 962Water용매HCID 6228
Dimethylformamide
용매

실험 절차

To a solution of 2-bromo-hexanoic acid methyl ester (0.500 g, 2.404 mmol) and 4-fluoro-3-methylphenol (0.303 g, 2.404 mmol) in 15 mL of DMF, was added K2CO3 (1.661 g, 12.020 mmol). After stirring at room temperature under N2 for 88 h, the reaction mixture was diluted with 60 mL of water and extracted with dichloromethane (60 mL×3). The organic extracts were combined and dried over anhydrous Na2SO4. After removing the solvent under reduced pressure, the product was isolated by Flash chromatography (silica gel) eluting with 0-20% ethyl acetate/hexanes to give the title compound as yellow oil (0.467 g, 76% yield). LC-MS: tR=10.5 min; m/z 255 (M+H)+.

후처리

  1. extractionextracted with dichloromethane (60 mL×3)
  2. dry with materialdried over anhydrous Na2SO4
  3. customAfter removing the solvent under reduced pressure
  4. customthe product was isolated by Flash chromatography (silica gel)
  5. washeluting with 0-20% ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-bbcc6eb5f8ad40e4b640f7efd6e964d9
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879911B2

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