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Stannous chloride dihydrate → tert-butyl N-((3-aminophenyl)methyl)carbamate

HRID 840589
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HRID 840589 반응식
[C:1]([O:5][C:6]([NH:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([N+:16]([O-])=O)[CH:11]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].O.O.[Sn](Cl)Cl>CN(C)C=O>[C:1]([O:5][C:6]([NH:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([NH2:16])[CH:11]=1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 61436Stannous chloride dihydrateHCID 22620025Tert-butyl 3-nitrobenzylcarbamate

생성물 1

HCID 10775412tert-butyl N-((3-aminophenyl)methyl)carbamate수율 100.3%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of N-(t-butyloxycarbonyl)-3-nitrobenzylamine (13.8 g, 54.7 mmol) in dimethylformamide (200 mL) was added tin(II) chloride dihydrate (74.1 g, 328 mmol) and the reaction was stirred at room temperature for 48 hours. The dimethylformamide was removed under vacuum. The residue was resuspended in dichloromethane (300 ml), washed with brine (200 mL), filtered through a celite pad, and the solvent removed to provide 12.2 g of the title compound. (100%).

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후처리

  1. customThe dimethylformamide was removed under vacuum
  2. washwashed with brine (200 mL)
  3. filtrationfiltered through a celite pad
  4. customthe solvent removed

출처 및 근거

ORD 기록
ord-a48ee9c049854b20952d0b9624409700
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06369070B1

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