Hydrochloric Acid → 6-Iodoindane-5-carbaldehyde

HRID 604612노트

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HRID 604612 반응식
[I:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][CH2:7][CH2:8]2)=[CH:4][C:3]=1[C:11]#N.[H-].C([Al+]CC(C)C)C(C)C.C1(C)C=CC=CC=1.Cl.CC[O:33]CC>C(Cl)Cl>[I:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][CH2:7][CH2:8]2)=[CH:4][C:3]=1[CH:11]=[O:33]

참가 물질

7

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온도
-78 °C

실험 절차

To a solution of 6-iodoindane-5-carbonitrile (36.5 mg, 0.136 mmol) in CH2Cl2 (1.0 mL) under N2 at −78° C. was added a solution of 1N diisobutyl aluminum hydride in toluene (272 μL, 0.272 mmol) dropwise. The reaction was stirred at −78° C. for 15 min. Keeping the temperature at −78° C., another two portions of diisobutyl aluminum hydride (100 μL each) were added until the starting material disappeared by TLC. The reaction mixture was poured into 2N HCl (45 mL) and diluted with Et2O. The mixture was stirred for 0.5 h. The Et2O layer was separated. The aqueous layer was extracted with Et2O (2×). The organic extracts were combined, dried (Na2SO4) and concentrated in vacuo. The residue was purified by flash chromatography (Si, hexanes/EtOAc) to afford 6-iodoindane-5-carbaldehyde. 1H NMR (500 MHz, CDCl3) δ 10.08 (s, 1H), 7.83 (s, 1H), 7.79 (s, 1H), 2.98 (t, J=7.5 Hz, 2H), 2.94 (t, J=7.5 Hz, 2H,), 2.19-2.13 (m, 2H).

후처리

  1. customat −78° C.
  2. stirringThe mixture was stirred for 0.5 h
  3. customThe Et2O layer was separated
  4. extractionThe aqueous layer was extracted with Et2O (2×)
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by flash chromatography (Si, hexanes/EtOAc)

출처 및 근거

ORD 기록
ord-ae6b5fda49f84e4186573fae51776f44
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07910592B2

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