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Hydrochloric Acid → 2-Methoxy-5-(1,1,2,2,2-pentafluoroethyl)benzaldehyde

HRID 1634336
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HRID 1634336 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([F:15])([F:14])[C:10]([F:13])([F:12])[F:11])=[CH:5][C:4]=1[CH:16]1OCCC[O:17]1.Cl>CC(C)=O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([F:14])([F:15])[C:10]([F:11])([F:12])[F:13])=[CH:5][C:4]=1[CH:16]=[O:17]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 18677628HCID 18677628, 화합물

생성물 1

HCID 186776122-Methoxy-5-(1,1,2,2,2-pentafluoroethyl)benzaldehyde수율 33.8%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a stirred solution of Compound 39 (1.0 g) in acetone (30 ml) was added conc. HCl (4 ml) at room temperature. The reaction mixture was stirred at room temperature for 5 h. The solvent was evaporated in vacuo and the residue was extracted with ether. The combined solution was washed with sat. NaHCO3 aq. , and brine, dried(MgSO4) and concentrated in vacuo to give crude product (790 mg) as a yellow solid. The crude product was purified by column chromatography on silica gel with hexane-isopropyl ether(10:1-3:1) to give Compound 40 (275 mg) as a pale yellow solid.

후처리

  1. customThe solvent was evaporated in vacuo
  2. extractionthe residue was extracted with ether
  3. washThe combined solution was washed with sat. NaHCO3 aq. , and brine, dried(MgSO4)
  4. concentrationconcentrated in vacuo
  5. customto give crude product (790 mg) as a yellow solid
  6. customThe crude product was purified by column chromatography on silica gel with hexane-isopropyl ether(10:1-3:1)

출처 및 근거

ORD 기록
ord-700a2257937c400f89997775bfe508d2
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06506775B1

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