Tetrahydrofuran → Ethyl 3-chloro-4-(2-methylpropyl)benzoate

HRID 2189747

반응식

HRID 2189747 반응식
[Br-].[CH2:2]([Zn+])[CH:3]([CH3:5])[CH3:4].C1COCC1.Br[C:13]1[CH:23]=[CH:22][C:16]([C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:15][C:14]=1[Cl:24]>>[Cl:24][C:14]1[CH:15]=[C:16]([CH:22]=[CH:23][C:13]=1[CH2:2][CH:3]([CH3:5])[CH3:4])[C:17]([O:19][CH2:20][CH3:21])=[O:18]

참가 물질

4

반응물 3

HCID 8028TetrahydrofuranHCID 12594301Ethyl 4-bromo-3-chlorobenzoateHCID 178448254HCID 178448254, 화합물

생성물 1

HCID 59316731Ethyl 3-chloro-4-(2-methylpropyl)benzoate

실험 절차

A solution of isobutylzinc bromide in THF (0.5 M, 30 mL, 15.0 mmol) was added under argon to ethyl 4-bromo-3-chlorobenzoate (D16) (2.00 g, 7.60 mmol) and then 1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride dichloromethane complex (930 mg, 1.14 mmol) was added. The reaction was heated to reflux for 4.5 h. The mixture concentrated in vacuo and the residue partitioned between ethyl acetate (125 mL) and water (125 mL). A solid formed, which was filtered off and discarded. The organic layer was washed with water (100 mL), dried (phase separator) and concentrated in vacuo. The crude product was purified by silica chromatography, eluting with 0-5% EtOAc in hexane over 30 minutes to give the title compound as a colourless oil (1.76 g, 7.33 mmol). δH (d6-DMSO, 400 MHz): 7.91 (1H, d), 7.80 (1H, dd), 7.46 (1H, d), 4.30 (2H, q), 2.66 (2H, d), 1.88-2.01 (1H, m), 1.32 (3H, t), 0.89 (6H, d).

후처리

  1. addition1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride dichloromethane complex (930 mg, 1.14 mmol) was added
  2. temperatureThe reaction was heated
  3. temperatureto reflux for 4.5 h
  4. concentrationThe mixture concentrated in vacuo
  5. customthe residue partitioned between ethyl acetate (125 mL) and water (125 mL)
  6. customA solid formed
  7. filtrationwhich was filtered off
  8. washThe organic layer was washed with water (100 mL)
  9. customdried (phase separator)
  10. concentrationconcentrated in vacuo
  11. customThe crude product was purified by silica chromatography
  12. washeluting with 0-5% EtOAc in hexane over 30 minutes

출처 및 근거

ORD 기록
ord-e097eab6fd8141a5a56cf02e82c39a73
출처 데이터셋
uspto-grants-2012_12
특허 번호
US08324254B2

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