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Methanol → Methyl 2-chloro-5-fluoro-4-methylbenzoate

HRID 1697339
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HRID 1697339 반응식
Br[C:2]1[CH:7]=[C:6]([F:8])[C:5]([CH3:9])=[CH:4][C:3]=1[Cl:10].C(N(CC)C(C)C)(C)C.CO.[C:22]([O:25][CH2:26]C)(=[O:24])C>C1C=CC([PH+]([C]2[CH][CH][CH][CH]2)C2C=CC=CC=2)=CC=1.C1C=CC([PH+]([C]2[CH][CH][CH][CH]2)C2C=CC=CC=2)=CC=1.C(Cl)Cl.Cl[Pd]Cl.[Fe]>[CH3:26][O:25][C:22](=[O:24])[C:2]1[CH:7]=[C:6]([F:8])[C:5]([CH3:9])=[CH:4][C:3]=1[Cl:10]
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참가 물질

6

반응물 4

HCID 887MethanolHCID 8857Ethyl AcetateHCID 81531DiisopropylethylamineHCID 27732721-Bromo-2-chloro-5-fluoro-4-methylbenzene

생성물 1

HCID 66688847Methyl 2-chloro-5-fluoro-4-methylbenzoate

시약·촉매·용매 1

HCID 53485975CID 53485975
촉매
2회

반응 조건

온도
90 °C

실험 절차

To a solution of 1-bromo-2-chloro-5-fluoro-4-methylbenzene (70 g) dissolved in ethyl acetate (400 mL) was added N,N-diisopropylethylamine (161 mL), dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (5.15 g) and methanol (120 mL). The resulting mixture was stirred at 90° C. for 24 h under carbon monoxide (4 bar) in a 1.5 L autoclave. Further dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (2.57 g) was added and the reaction heated at 90° C. for a further 3 h. The cooled reaction mixture was evaporated to dryness and the residue purified by silica chromatography, eluting with 50% dichloromethane in iso-hexane to give the subtitle compound (57.7 g).

후처리

  1. temperaturethe reaction heated at 90° C. for a further 3 h
  2. customThe cooled reaction mixture
  3. customwas evaporated to dryness
  4. customthe residue purified by silica chromatography
  5. washeluting with 50% dichloromethane in iso-hexane

출처 및 근거

ORD 기록
ord-72ff7a6f74804f4a9399ff4480837806
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163905B2

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