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Methane → 2-amino-5-(N-ethoxycarbonylamino)phenol

HRID 1885496
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인쇄 미리보기

반응식

HRID 1885496 반응식
[CH2:1]([O:3][C:4]([NH:6][C:7]1[CH:8]=[CH:9][C:10]([NH:14]C(OCC2C=CC=CC=2)=O)=[C:11]([OH:13])[CH:12]=1)=[O:5])[CH3:2].C1CCCCC=1.C>C(O)C>[NH2:14][C:10]1[CH:9]=[CH:8][C:7]([NH:6][C:4]([O:3][CH2:1][CH3:2])=[O:5])=[CH:12][C:11]=1[OH:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 297MethaneHCID 8079CyclohexeneHCID 147457375-(Ethoxycarbonylamino)-2-(benzyloxycarbonylamino)phenol

생성물 1

HCID 147457382-amino-5-(N-ethoxycarbonylamino)phenol

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

0.06 mole (20 g) of 5-(ethoxycarbonylamino) -2-(benzyloxycarbonylamino)phenol in 60 ml of 96° strength ethanol to which 40 ml of cyclohexene and 4 g of palladinized charcoal (10% palladium) are added is heated to reflux for 30 minutes. After removal of the catalyst by filtration while hot, the expected product is precipitated by adding 17.5 ml of ethanolic hydrochloric acid (7M) to the cooled filtrate. After drying, analysis of the product obtained gives the following results:

후처리

  1. temperatureis heated
  2. temperatureto reflux for 30 minutes
  3. customAfter removal of the catalyst
  4. filtrationby filtration while hot, the expected product
  5. customis precipitated
  6. additionby adding 17.5 ml of ethanolic hydrochloric acid (7M) to the cooled filtrate
  7. customAfter drying
  8. customanalysis of the product obtained
  9. customgives the
  10. customfollowing results

출처 및 근거

ORD 기록
ord-5ce0d57a12824bf7b996ac73d8b112f4
출처 데이터셋
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05145483

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