Iodine → 3-Iodobenzaldehyde diethyl acetal

HRID 52172노트

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HRID 52172 반응식
[CH2:1]([O:3][CH:4]([O:12][CH2:13][CH3:14])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7](Br)[CH:6]=1)[CH3:2].C([Li])CCC.[I:20]I>C1COCC1>[CH2:1]([O:3][CH:4]([O:12][CH2:13][CH3:14])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([I:20])[CH:6]=1)[CH3:2]

참가 물질

5

실험 절차

To a stirred -78° C. solution of 3-bromobenzaldehyde diethyl acetal, prepared as in step 1, (1.0 g, 3.8 mmol) in THF (10 mL) was added n-butyllithium (1.7 mL, 4.25 mmol, 2.5M in hexanes). The cold reaction mixture was stirred 0.5 hours followed by the addition of a THF (5 mL) solution of iodine (1.09 g, 4.25 mmol). The ice bath was removed and the reaction allowed to warm to ambient temperature. Saturated NH4Cl was added and the mixture diluted with hexanes. The organic layer was washed with brine, dried (MgSO4) and concentrated under reduced pressure to give a residue which was purified by column chromatography on silica gel eluting with 5% ethyl acetate-hexanes to afford 1.0 g of 3-iodobenzaldehyde diethyl acetal.

후처리

  1. customThe cold reaction mixture
  2. customThe ice bath was removed
  3. additionSaturated NH4Cl was added
  4. additionthe mixture diluted with hexanes
  5. washThe organic layer was washed with brine
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated under reduced pressure
  8. customto give a residue which
  9. customwas purified by column chromatography on silica gel eluting with 5% ethyl acetate-hexanes

출처 및 근거

ORD 기록
ord-6efb15823f2049789cc24967e559a6a3
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05616596

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