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benzyl N-(2-hydroxy-4-nitrophenyl)carbamate → 5-Amino-2-(benzyloxycarbonylamino)phenol

HRID 1885493
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반응식

HRID 1885493 반응식
[CH2:1]([O:8][C:9]([NH:11][C:12]1[CH:17]=[CH:16][C:15]([N+:18]([O-])=O)=[CH:14][C:13]=1[OH:21])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H][H]>C(O)C.[Ni]>[NH2:18][C:15]1[CH:16]=[CH:17][C:12]([NH:11][C:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[O:10])=[C:13]([OH:21])[CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14745732benzyl N-(2-hydroxy-4-nitrophenyl)carbamateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 147457335-Amino-2-(benzyloxycarbonylamino)phenol

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

0.53 mole (153 g) of 2-(benzyloxycarbonylamino) -5-nitrophenol in 1 liter of ethanol is subjected to a hydrogen pressure of 8×105 pascals (8 bars) in an autoclave in the presence of 60 g of Raney nickel (water content 50%). After 1 hour at 65° C., the reaction medium is filtered while hot in order to remove the catalyst. On cooling the filtrate, the expected product crystallizes. After draining and drying, the product obtained is recrystallized in 96° strength ethanol. It melts at 148° C.

후처리

  1. filtrationthe reaction medium is filtered while hot in order
  2. customto remove the catalyst
  3. temperatureOn cooling the filtrate
  4. customthe expected product crystallizes
  5. customdrying
  6. customthe product obtained
  7. customis recrystallized in 96° strength ethanol

출처 및 근거

ORD 기록
ord-f470ef3bc6324a3f891ce7bc2cfc7601
출처 데이터셋
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05145483

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