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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Peracetic Acid → HCID 19010447, 화합물

HRID 903862
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HRID 903862 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:12]=[CH:13][CH:14]=1)[O:5][C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1.C(OO)(=[O:17])C>C(O)(=O)C>[F:1][C:2]1[CH:3]=[C:4]([CH:12]=[CH:13][CH:14]=1)[O:5][C:6]1[CH:7]=[N+:8]([O-:17])[CH:9]=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6585Peracetic AcidHCID 126734843-(3-Fluorophenoxy)pyridine

생성물 1

HCID 19010447HCID 19010447, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

A solution of 32 g of 3-(3-fluorophenoxy)pyridine [Fr. Pat. No. 1,472,619 (1967)] in 50 ml of glacial acetic acid is treated with 35 g of 40% peracetic acid in acetic acid and the mixture is refluxed 16 hours. The mixture is concentrated at reduced pressure and the oil is dissolved in 250 ml of dichloromethane. The dichloromethane solution is washed with excess 10% sodium hydroxide solution. The solution is dried and concentrated to dryness to yield 3-(3-fluorophenoxy)pyridine 1-oxide, m.p. 63°-66° C.

후처리

  1. temperaturethe mixture is refluxed 16 hours
  2. concentrationThe mixture is concentrated at reduced pressure
  3. dissolutionthe oil is dissolved in 250 ml of dichloromethane
  4. washThe dichloromethane solution is washed with excess 10% sodium hydroxide solution
  5. customThe solution is dried
  6. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-83e20b08ca0448669fb98d659cc7192b
출처 데이터셋
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04229457

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