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Bromine → 4-Bromo-1-(methylthio)-2-(trifluoromethyl)-benzene

HRID 748899
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반응식

HRID 748899 반응식
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]([F:12])([F:11])[F:10].[Br:13]Br.[Cl-].[Al+3].[Cl-].[Cl-].S([O-])([O-])(=O)=S.[Na+].[Na+]>[Fe].C(OCC)(=O)C.O.ClCCl>[Br:13][C:6]1[CH:7]=[CH:8][C:3]([S:2][CH3:1])=[C:4]([C:9]([F:10])([F:11])[F:12])[CH:5]=1
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참가 물질

9

반응물 4

HCID 24408BromineHCID 24477Sodium ThiosulfateHCID 27607832-TrifluoromethylthioanisoleHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 223153184-Bromo-1-(methylthio)-2-(trifluoromethyl)-benzene수율 83%

시약·촉매·용매 4

HCID 23925Iron촉매
HCID 962Water용매
HCID 6344Dichloromethane용매
HCID 8857Ethyl Acetate용매

실험 절차

Combine 1-methylsulfanyl-2-trifluoromethyl-benzene (3.5 g, 18 mmol), iron (100 mg, 1.79 mmol), bromine (0.95 mL, 18 mmol), aluminum chloride (242 mg, 1.8 mmol) and dichloromethane (50 mL) and stir for 2 hours. Add water (10 mL), aqueous saturated sodium thiosulfate (100 mL) and ethyl acetate (100 mL). Separate the organic layer and wash with brine, dry with MgSO4, filter and concentrate in vacuo. Chromatograph the residue on a SiO2 column eluting with hexane to give 3.6 g of 4-bromo-1-methylsulfanyl-2-trifluoromethyl-benzene (83%).

후처리

  1. customSeparate the organic layer
  2. washwash with brine
  3. dry with materialdry with MgSO4
  4. filtrationfilter
  5. concentrationconcentrate in vacuo
  6. washChromatograph the residue on a SiO2 column eluting with hexane

출처 및 근거

ORD 기록
ord-364a549288a3412aa83d2f8b162fff16
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07399867B2

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