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Trimethylsulfonium iodide → 2,2-Bis(3-bromophenyl)oxirane

HRID 1429269
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인쇄 미리보기

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HRID 1429269 반응식
[CH3:1]C([O-])(C)C.[K+].[Br:7][C:8]1[CH:9]=[C:10]([C:14]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([Br:22])[CH:17]=2)=[O:15])[CH:11]=[CH:12][CH:13]=1.[I-].C[S+](C)C>CS(C)=O.C(OCC)(=O)C>[Br:7][C:8]1[CH:9]=[C:10]([C:14]2([C:16]3[CH:21]=[CH:20][CH:19]=[C:18]([Br:22])[CH:17]=3)[CH2:1][O:15]2)[CH:11]=[CH:12][CH:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 75127Trimethylsulfonium iodideHCID 12731928Bis(3-bromophenyl)methanoneHCID 23665647Potassium tert-butoxide

생성물 1

HCID 580319912,2-Bis(3-bromophenyl)oxirane

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 8857Ethyl Acetate용매

반응 조건

온도
30 °C

실험 절차

KOt-Bu (2.72 g, 24.26 mmol) was added to a stirred suspension of bis(3-bromophenyl)methanone (7.5 g, 22.06 mmol) and trimethylsulfonium iodide (4.50 g, 22.06 mmol) in DMSO (20 mL) and the resulting mixture was stirred at 30° C. for 8 h. The mixture was diluted with ethyl acetate (500 mL), washed with water (500 mL×3) and brine (500 mL). The organic layer was separated and evaporated in vacuo to afford the title compound which was used directly without further purification.

후처리

  1. washwashed with water (500 mL×3) and brine (500 mL)
  2. customThe organic layer was separated
  3. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-66921278e40d4a5d8e2defeaa44e5cfb
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08937150B2

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