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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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m-Chloroperbenzoic acid → 5-(Oxiran-2-yl)-2,1,3-benzoxadiazole

HRID 1502054
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HRID 1502054 반응식
[CH:1]([C:3]1[CH:11]=[CH:10][C:6]2=[N:7][O:8][N:9]=[C:5]2[CH:4]=1)=[CH2:2].C1C=C(Cl)C=C(C(OO)=[O:20])C=1>C(Cl)Cl>[O:20]1[CH2:2][CH:1]1[C:3]1[CH:11]=[CH:10][C:6]2=[N:7][O:8][N:9]=[C:5]2[CH:4]=1
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 595687205-Ethenyl-2,1,3-benzoxadiazole

생성물 1

HCID 595686615-(Oxiran-2-yl)-2,1,3-benzoxadiazole

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 5-ethenyl-2,1,3-benzoxadiazole (1.80 g, 12.3 mmol) in DCM (20 mL) was slowly added m-CPBA (3.8 g, 22 mmol) at 0° C. The flask was warmed to room temperature; the mixture was then stirred for 12 hours. TLC as well as LC indicated that reaction had gone to completion. The mixture was washed with aqueous Na2S2O3, NaHCO3, and water. The organic layers was washed with brine and then concentrated. The residue was purified over silica gel to afford the title compound.

후처리

  1. customat 0° C
  2. customTLC as well as LC indicated that reaction
  3. washThe mixture was washed with aqueous Na2S2O3, NaHCO3, and water
  4. washThe organic layers was washed with brine
  5. concentrationconcentrated
  6. customThe residue was purified over silica gel

출처 및 근거

ORD 기록
ord-9b1e90322f5a456fb9af78d4c1cf850a
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09206199B2

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