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Methanone, (2-nitrophenyl)phenyl- → 2-Aminobenzophenone

HRID 965272
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인쇄 미리보기

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HRID 965272 반응식
[N+:1]([C:4]1[CH:17]=[CH:16][CH:15]=[CH:14][C:5]=1[C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[O:7])([O-])=O>C1COCC1.CO.O>[NH2:1][C:4]1[CH:17]=[CH:16][CH:15]=[CH:14][C:5]=1[C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[O:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 137514Methanone, (2-nitrophenyl)phenyl-

생성물 1

HCID 760802-Aminobenzophenone

시약·촉매·용매 3

HCID 887Methanol용매HCID 962Water용매HCID 8028Tetrahydrofuran용매

반응 조건

온도
70 °C

실험 절차

A mixture of nitrobenzophenone resin, 3-Scheme 6, (950 mg), NaSH (1.0 g) in THF (10 mL), MeOH (5 mL), water (5 mL) was heated in an oil bath at 70° C. for 16 h. The mixture was cooled, filtered and washed with methanol, water, methylene chloride and finally with methanol. Drying at 60° (in vacuo gave a slight yellow resin. Recovered (900 mg). IR 1640 (broad).

후처리

  1. temperatureThe mixture was cooled
  2. filtrationfiltered
  3. washwashed with methanol, water, methylene chloride and finally with methanol
  4. customDrying at 60° (in vacuo
  5. customgave a slight yellow resin
  6. customRecovered (900 mg)

출처 및 근거

ORD 기록
ord-98e42d8282b748fabdb770bcde906419
출처 데이터셋
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05773512

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