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Methane, dichloromethoxy- → 4-Chloro-5-ethyl-2-fluorobenzaldehyde

HRID 2105069
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HRID 2105069 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][CH3:10].Cl[CH:12](Cl)[O:13]C>C(Cl)Cl.Cl[Ti](Cl)(Cl)Cl>[Cl:1][C:2]1[C:3]([CH2:9][CH3:10])=[CH:4][C:5]([CH:12]=[O:13])=[C:6]([F:8])[CH:7]=1
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참가 물질

5

반응물 2

HCID 21004Methane, dichloromethoxy-HCID 213412082-Chloro-1-ethyl-4-fluorobenzene

생성물 1

HCID 578038014-Chloro-5-ethyl-2-fluorobenzaldehyde

시약·촉매·용매 2

HCID 24193Titanium Tetrachloride촉매HCID 6344Dichloromethane용매

실험 절차

TiCl4 (0.90 mL) was added to 2-chloro-1-ethyl-4-fluorobenzene (645 mg, 4.1 mmol) at 0° C. and stirred to 10 min. Dichloro(methoxy)methane (0.725 mL) was added and the mixture was stirred overnight at ambient temperature. The mixture was diluted with CH2Cl2 (50 mL) and poured onto crushed ice (40 g). After stirring 30 min the layers were separated. The organic layer was washed with H2O (2×), brine (2×), dried (Na2SO4) and concentrated. Purification by flash chromatography (hexanes, EtOAc) yielded 440 mg of intermediate 390.2 as a light brown oil. 1H NMR (400 MHz, CDCl3) δ ppm 1.18 (t, J=7.58 Hz, 3H) 2.69 (q, J=7.58 Hz, 2H) 7.05-7.29 (m, 1H) 7.67 (m, 1H) 10.23 (s, 1H).

후처리

  1. stirringthe mixture was stirred overnight at ambient temperature
  2. additionpoured
  3. stirringAfter stirring 30 min the layers
  4. customwere separated
  5. washThe organic layer was washed with H2O (2×), brine (2×)
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated
  8. customPurification by flash chromatography (hexanes, EtOAc)

출처 및 근거

ORD 기록
ord-01167c6df1c3458eb5b8d9ccfe6f9d00
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07576098B2

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