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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Isopropanol → HCID 54105304, 화합물

HRID 1448140
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HRID 1448140 반응식
[F:1][C:2]1[CH:14]=[CH:13][CH:12]=[CH:11][C:3]=1[O:4][C:5]1[CH:6]=[N:7][CH:8]=[CH:9][CH:10]=1.C(OO)(=[O:17])C.C(O)(C)C>C(O)(=O)C>[F:1][C:2]1[CH:14]=[CH:13][CH:12]=[CH:11][C:3]=1[O:4][C:5]1[CH:6]=[N+:7]([O-:17])[CH:8]=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 6585Peracetic AcidHCID 12673483HCID 12673483, 화합물

생성물 1

HCID 54105304HCID 54105304, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

A solution of 30 g of 3-(o-fluorophenoxy)pyridine in 50 ml of glacial acetic acid is treated at 35° C. with 33 g of 40% peracetic acid in acetic acid in four portions. The mixture is stirred for 16 hours, refluxed 1 hour and 50 ml of isopropanol is added and the heating continued at 95° C. for 1 hour. The mixture is concentrated at reduced pressure and is dissolved in 300 ml of dichloromethane. The solution is washed with excess 25% sodium hydroxide solution. The dichloromethane solution is dryed over anhydrous MgSO4, filtered and concentrated at reduced pressure. The 3-(o-fluorophenoxy)-pyridine N-oxide crystallizes, mp 89°-95° C.

후처리

  1. temperaturerefluxed 1 hour
  2. waitthe heating continued at 95° C. for 1 hour
  3. concentrationThe mixture is concentrated at reduced pressure
  4. dissolutionis dissolved in 300 ml of dichloromethane
  5. washThe solution is washed with excess 25% sodium hydroxide solution
  6. filtrationfiltered
  7. concentrationconcentrated at reduced pressure
  8. customThe 3-(o-fluorophenoxy)-pyridine N-oxide crystallizes

출처 및 근거

ORD 기록
ord-24e54f018a224afdb3966ba6e9232599
출처 데이터셋
uspto-grants-1979_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04179563

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