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Chloromethyl Methyl Ether → 3-Bromo-5-fluoro-4-methoxymethoxybenzoic acid methyl ester

HRID 423244
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인쇄 미리보기

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HRID 423244 반응식
[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[C:8]([F:10])[C:7]([OH:11])=[C:6]([Br:12])[CH:5]=1.C(=O)([O-])[O-].[K+].[K+].[CH3:20][O:21][CH2:22]Cl>CC(C)=O.C(OCC)(=O)C>[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[C:8]([F:10])[C:7]([O:11][CH2:20][O:21][CH3:22])=[C:6]([Br:12])[CH:5]=1
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참가 물질

6

반응물 3

HCID 7864Chloromethyl Methyl EtherHCID 11430Potassium CarbonateHCID 57467610Methyl 3-bromo-5-fluoro-4-hydroxybenzoate

생성물 1

HCID 586297383-Bromo-5-fluoro-4-methoxymethoxybenzoic acid methyl ester수율 81.1%

시약·촉매·용매 2

HCID 180Acetone용매HCID 8857
Ethyl Acetate
용매

실험 절차

To a solution of 3-bromo-5-fluoro-4-hydroxybenzoic acid methyl ester (637 mg) in acetone (7 mL) were added potassium carbonate (708 mg) and chloromethyl methyl ether (412 mg), and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=9:1, v/v) to give the title compound (608 mg).

후처리

  1. washwashed with water and saturated brine
  2. dry with materialdried over anhydrous sodium sulfate
  3. concentrationconcentrated in vacuo
  4. customThe residue was purified by column chromatography on silica gel (hexane

출처 및 근거

ORD 기록
ord-b88afdcd891b4a598cd288cb275ead05
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08101774B2

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