Stannous chloride dihydrate → 2-Amino-4,6-di-tert-butylphenol

HRID 423813노트

반응식

HRID 423813 반응식
[C:1]([C:5]1[CH:10]=[C:9]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:8]=[C:7]([N+:15]([O-])=O)[C:6]=1[OH:18])([CH3:4])([CH3:3])[CH3:2].O.O.Cl[Sn]Cl.C([O-])(O)=O.[Na+]>CCO.CCOC(C)=O.O>[NH2:15][C:7]1[C:6]([OH:18])=[C:5]([C:1]([CH3:3])([CH3:2])[CH3:4])[CH:10]=[C:9]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:8]=1

참가 물질

7

반응물 3

HCID 61436Stannous chloride dihydrateHCID 516892Sodium BicarbonateHCID 6168972,4-Bis(tert-butyl)-6-nitrophenol

생성물 1

HCID 3245552-Amino-4,6-di-tert-butylphenol

시약·촉매·용매 3

HCID 702Ethanol용매HCID 962Water용매HCID 8857Ethyl Acetate용매

실험 절차

A solution of 2,4-di-tert-butyl-6-nitro-phenol (27 mg, 0.11 mmol) and SnCl2.2H2O (121 mg, 0.54 mmol) in EtOH (1.0 mL) was heated in microwave oven at 100° C. for 30 min. The mixture was diluted with EtOAc and water, basified with sat. NaHCO3 and filtered through Celite. The organic layer was separated and dried over Na2SO4. Solvent was removed by evaporation to provide 6-amino-2,4-di-tert-butyl-phenol (C-8), which was used without further purification. HPLC ret. time 2.74 min, 10-99% CH3CN, 5 min run; ESI-MS 222.5 m/z (MH+).

후처리

  1. filtrationfiltered through Celite
  2. customThe organic layer was separated
  3. dry with materialdried over Na2SO4
  4. customSolvent was removed by evaporation

출처 및 근거

ORD 기록
ord-e5a671c3fca942dc8d579a2a60d33f7c
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08101767B2

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