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4,4'-Dichlorobenzophenone → alpha,alpha-bis(4-Chlorophenyl)oxiranemethanol

HRID 845339
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HRID 845339 반응식
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.C([Mg]Br)=C.[CH2:21]1[CH2:25][O:24]CC1.[NH4+].[Cl-]>CCOCC>[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=2)([CH:21]2[CH2:25][O:24]2)[OH:7])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 70344,4'-DichlorobenzophenoneHCID 25517Ammonium ChlorideHCID 178420667HCID 178420667, 화합물

생성물 1

HCID 13534918alpha,alpha-bis(4-Chlorophenyl)oxiranemethanol

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To a solution of 6 g of 4,4'-dichlorobenzophenone in 200 mL of ether was added 30 mL of 1.4M vinylmagnesium bromide/THF at 0°. After being stirred at 25° for 20 minutes, the mixture was poured onto aqueous NH4Cl, partitioned, washed with brine, dried (MgSO4), filtered, and concentrated. The crude adduct was allowed to stand in 50 mL of methylene chloride with 5.8 g of m-chloroperbenzoic acid for 3 days at 25°. The mixture was diluted with CH2Cl2, washed with aqueous NaHSO3, aqueous NaHCO3, brine, dried (Na2SO4), concentrated, and chromatographed (150 mL SiO2 /30% CH2Cl2 in hexane) to provide 2.9 g of the title compound (after washing the concentrated fractions with pentane), m.p. 87°-88°.

후처리

  1. custompartitioned
  2. washwashed with brine
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. waitto stand in 50 mL of methylene chloride with 5.8 g of m-chloroperbenzoic acid for 3 days at 25°
  7. additionThe mixture was diluted with CH2Cl2
  8. washwashed with aqueous NaHSO3, aqueous NaHCO3, brine
  9. dry with materialdried (Na2SO4)
  10. concentrationconcentrated
  11. customchromatographed (150 mL SiO2 /30% CH2Cl2 in hexane)

출처 및 근거

ORD 기록
ord-58760e6be0794cd2a898e62643450437
출처 데이터셋
uspto-grants-1988_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04758262

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