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m-Chloroperbenzoic acid → 5-(oxiran-2-yl)-2-benzofuran-1(3H)-one

HRID 2175759
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HRID 2175759 반응식
[CH:1]([C:3]1[CH:12]=[CH:11][C:6]2[C:7](=[O:10])[O:8][CH2:9][C:5]=2[CH:4]=1)=[CH2:2].C1C=C(Cl)C=C(C(OO)=[O:21])C=1>C(Cl)Cl>[O:21]1[CH2:2][CH:1]1[C:3]1[CH:12]=[CH:11][C:6]2[C:7](=[O:10])[O:8][CH2:9][C:5]=2[CH:4]=1
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acid2회HCID 211063135-ethenyl-2-benzofuran-1(3H)-one

생성물 1

HCID 595687155-(oxiran-2-yl)-2-benzofuran-1(3H)-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

5-Ethenyl-2-benzofuran-1(3H)-one (28.4 g, 177 mmol) was dissolved in DCM (400 mL) then mCPBA (47.7 g, 213 mmol) was added. The mixture was stirred at room temperature overnight. Some starting olefin remained. Another 25 g of mCPBA was added and the mixture was stirred overnight. The mixture was poured into ice cold Na2SO3 solution (saturated). The layers were separated and the organic layer was washed with 5% NaOH solution, brine, then was dried (MgSO4). The crude product was purified by MPLC (330 g column, eluting with 40% EtOAc/hexane, 2 L, then with 45% EtOAc/hexane, 2 L, to afford 5-(oxiran-2-yl)-2-benzofuran-1(3H)-one. LC-MS: M+1=177.

후처리

  1. stirringthe mixture was stirred overnight
  2. additionThe mixture was poured into ice cold Na2SO3 solution (saturated)
  3. customThe layers were separated
  4. washthe organic layer was washed with 5% NaOH solution, brine
  5. dry with materialwas dried (MgSO4)
  6. customThe crude product was purified by MPLC (330 g column
  7. washeluting with 40% EtOAc/hexane, 2 L

출처 및 근거

ORD 기록
ord-8dbc2dac70874230a568adc472040142
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062070B2

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