1,2-Dichloroethane → 5-Chloro-2-iodobenzaldehyde

HRID 1728143노트

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HRID 1728143 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([I:11])=[C:6]([CH:10]=1)[C:7](O)=[O:8].O1CCCC1.B.ClCCCl>O1CCCC1.O=[Mn]=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([I:11])=[C:6]([CH:10]=1)[CH:7]=[O:8]

참가 물질

6

실험 절차

To a solution of 5-chloro-2-iodo benzoic acid (4.92 g, 17 mmol) (TRANS) in anhydrous tetrahydrofuran (100 mL) at 0° C. was added borane tetrahydrofuran (1 M, 34 mL, 34 mmol) dropwise. The reaction mixture was then stirred at room temperature for 18 h. The mixture was concentrated and residue was partitioned between ethyl acetate and water. Organic layer was separated, washed with brine, dried over MgSO4, and concentrated to give a colorless oil. The oil was dissolved into 1,2-dichloroethane (50 mL), and activated MnO2 (15 g) was added. The mixture was then heated at reflux for 2 h, cooled to room temperature, and filtered through a short pad of celite. The filtrated was concentrated and purified by chromatography (EtOAc:hexanes=1;8) to give 5-chloro-2-Iodo-benzaldehyde as a white solid (Yield 5.5 g, 25%).

후처리

  1. concentrationThe mixture was concentrated
  2. customresidue was partitioned between ethyl acetate and water
  3. customOrganic layer was separated
  4. washwashed with brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated
  7. customto give a colorless oil
  8. additionwas added
  9. temperatureThe mixture was then heated
  10. temperatureat reflux for 2 h
  11. temperaturecooled to room temperature
  12. filtrationfiltered through a short pad of celite
  13. concentrationThe filtrated was concentrated
  14. custompurified by chromatography (EtOAc:hexanes=1;8)

출처 및 근거

ORD 기록
ord-e3e0f6e74898478bb0b8ad6c025148a1
출처 데이터셋
uspto-grants-2009_02
특허 번호
US07495007B2

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