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Water → Methyl 3-bromo-4-(difluoromethoxy)benzoate

HRID 1420835
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HRID 1420835 반응식
Cl[C:2]([F:9])([F:8])C(OCC)=O.[Br:10][C:11]1[CH:12]=[C:13]([CH:18]=[CH:19][C:20]=1[OH:21])[C:14]([O:16][CH3:17])=[O:15].C(=O)([O-])[O-].[K+].[K+].O>CN(C)C=O>[Br:10][C:11]1[CH:12]=[C:13]([CH:18]=[CH:19][C:20]=1[O:21][CH:2]([F:9])[F:8])[C:14]([O:16][CH3:17])=[O:15]
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6

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HCID 962WaterHCID 11430Potassium CarbonateHCID 67843Acetic acid, 2-chloro-2,2-difluoro-, ethyl esterHCID 4778958Methyl 3-bromo-4-hydroxybenzoate

생성물 1

HCID 18782607Methyl 3-bromo-4-(difluoromethoxy)benzoate수율 49.1%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

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온도
65 °C

실험 절차

Ethyl chlorodifluoroacetate (1.12 ml, 8.7 mmol) was added to a mixture of methyl 3-bromo-4-hydroxybenzoate (Description 64, 2.0 g, 8.7 mmol) and potassium carbonate (1.2 g, 8.7 mmol) in N,N-dimethylformamide (20 ml) and the mixture was heated at 65° C. for 16 h. The mixture was cooled, water (100 ml) was added and the mixture was extracted with ethyl acetate (2×100 ml). The combined organic fractions were dried (Na2SO4) and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with hexane/EtOAc (95:5) to give the title compound as a colorless solid (1.20 g, 49%). 1H NMR (250 MHz, CDCl3) δ8.31 (1 H, d, J 2.0 Hz), 8.22 (1 H, dd, J 8.5, 2.0 Hz), 7.05 (1 H, m), 6.61 (1 H, t, J 73 Hz), and 3.93 (3 H, s).

후처리

  1. temperatureThe mixture was cooled
  2. extractionthe mixture was extracted with ethyl acetate (2×100 ml)
  3. dry with materialThe combined organic fractions were dried (Na2SO4)
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was purified by column chromatography on silica gel
  6. washeluting with hexane/EtOAc (95:5)

출처 및 근거

ORD 기록
ord-ff789bc50d0c45f7a9d207a91ae837de
출처 데이터셋
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06071927

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