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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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m-Chloroperbenzoic acid → Furo[3,2-b]pyridine 4-oxide

HRID 1192402
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HRID 1192402 반응식
[O:1]1[C:9]2[C:4](=[N:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.C1C=C(Cl)C=C(C(OO)=[O:18])C=1>C(Cl)(Cl)Cl>[O:1]1[C:9]2[C:4](=[N+:5]([O-:18])[CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 12210217Furo(3,2-b)pyridine

생성물 1

HCID 10630536Furo[3,2-b]pyridine 4-oxide수율 88%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

To a solution of Furo[3,2-b]pyridine (1.5 g, 13.0 mmol) in CHCl3 (30 mL) was added MCPBA (2.9 g, 17.0 mmol). The mixture was stirred at room temperature for 16 hours. Then the mixture was filtered through a alumina (140 g, basic) and washed with ethyl acetate/hexane (1:1) and DCM/MeOH (20:1) to give Furo[3,2-b]pyridine 4-oxide (1.49 g, 88%). 1H NMR (CDCl3, 400 MHz) δ 8.25 (m, 1H), 7.81 (m, 1H), 7.51 (m, 1H), 7.23 (m, 1H).

후처리

  1. filtrationThen the mixture was filtered through a alumina (140 g, basic)
  2. washwashed with ethyl acetate/hexane (1:1) and DCM/MeOH (20:1)

출처 및 근거

ORD 기록
ord-9f3a2bcc15604a0da768bf3018928a71
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680114B2

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