Acetic Acid → Ethyl 4-(1-amino-2-methylpropyl)benzoate

HRID 1049088노트

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HRID 1049088 반응식
O[N:2]=[C:3]([C:7]1[CH:17]=[CH:16][C:10]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:9][CH:8]=1)[CH:4]([CH3:6])[CH3:5].C(O)(=O)C.[OH-].[NH4+].C(Cl)Cl>[Zn].CCOC(C)=O>[NH2:2][CH:3]([C:7]1[CH:17]=[CH:16][C:10]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:9][CH:8]=1)[CH:4]([CH3:5])[CH3:6]

참가 물질

7

실험 절차

To the crude ethyl 4-(1-(hydroxyimino)-2-methylpropyl)benzoate in a 100-mL round-bottom flask was added acetic acid (8 mL) and zinc dust (1.33 g, 20.3 mmol). The mixture was stirred at rt for 1 h, then filtered through a pad of Celite. The pad was rinsed with ethanol (50 mL). Combined filtrate was concentrated to give a solid. To the solid residue was added ammonium hydroxide (20 mL) and DCM (50 mL). The solution was stirred at rt for 10 min. After separation, the aqueous layer was extracted with DCM (2×50 mL). Combined organic phases were washed with brine, dried (MgSO4), and concentrated to give an oil. Flash column chromatography (EtOAc:hexanes:TEA, 20:80:2 to 100:0:2) afforded ethyl 4-(1-amino-2-methylpropyl)benzoate (0.563 g, 55%) as a clear oil. LC-MS: (FA) ES+ 222; 1H NMR (CDCl3, 300 MHz) δ7.99 (d, J=8.3 Hz, 2H), 7.36 (d, J=8.5 Hz, 2H), 4.37 (q, J=7.2 Hz, 2 μl), 3.68 (d, J=7.0 Hz, 1H), 1.86 (m, 1H), 1.39 (t, J=7.0 Hz, 3H), 0.96 (d, J=7.0 Hz, 3H), 0.77 (d, J=7.0 Hz, 3H).

후처리

  1. filtrationfiltered through a pad of Celite
  2. washThe pad was rinsed with ethanol (50 mL)
  3. concentrationCombined filtrate was concentrated
  4. customto give a solid
  5. stirringThe solution was stirred at rt for 10 min
  6. customAfter separation
  7. extractionthe aqueous layer was extracted with DCM (2×50 mL)
  8. washCombined organic phases were washed with brine
  9. dry with materialdried (MgSO4)
  10. concentrationconcentrated
  11. customto give an oil

출처 및 근거

ORD 기록
ord-041c685f2ea44ec8b4bddb7819e5fbad
출처 데이터셋
uspto-grants-2016_07
특허 번호
US09382197B2

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