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Acetic Acid → 4-((tert-Butyldimethylsilyl)oxy)benzene-1,2-diamine

HRID 920117
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인쇄 미리보기

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HRID 920117 반응식
[Si:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([NH2:15])=[C:11]([N+:16]([O-])=O)[CH:10]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].C(O)(=O)C>CCO.[Fe]>[Si:1]([O:8][C:9]1[CH:10]=[C:11]([NH2:16])[C:12]([NH2:15])=[CH:13][CH:14]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 120422994-(Tert-butyldimethylsilyl)oxy-2-nitroaniline

생성물 1

HCID 672786584-((tert-Butyldimethylsilyl)oxy)benzene-1,2-diamine

시약·촉매·용매 2

HCID 23925Iron촉매HCID 702Ethanol용매

실험 절차

The mixture of 4-(tert-butyldimethylsilyloxy)-2-nitrobenzenamine (0.5 g, 1.9 mmol), Fe powder (1.1 g, 19 mmol) and acetic acid (1.0 mL, 18 mmol) in EtOH (10 mL) was stirred at reflux for 4 hrs. The mixture was filtered through celite pad and the filtrate was concentrated.

후처리

  1. temperatureat reflux for 4 hrs
  2. filtrationThe mixture was filtered through celite pad
  3. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-64301a4e86764faaa072ab461b72ee38
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09273046B2

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