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N,N-Dimethylglycine → 1-Bromo-4-(4-methylphenoxy)benzene

HRID 1622770
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인쇄 미리보기

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HRID 1622770 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[Br:9][C:10]1[CH:15]=[CH:14][C:13](Br)=[CH:12][CH:11]=1.C(=O)([O-])[O-].[K+].[K+].CN(C)CC(O)=O>CN(C=O)C.[NH4+].[Cl-].[Cu]I>[Br:9][C:10]1[CH:15]=[CH:14][C:13]([O:8][C:5]2[CH:6]=[CH:7][C:2]([CH3:1])=[CH:3][CH:4]=2)=[CH:12][CH:11]=1
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참가 물질

8

반응물 4

HCID 673N,N-DimethylglycineHCID 2879P-CresolHCID 78041,4-DibromobenzeneHCID 11430Potassium Carbonate

생성물 1

HCID 221862981-Bromo-4-(4-methylphenoxy)benzene수율 65%

시약·촉매·용매 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)
촉매
HCID 6228Dimethylformamide용매
HCID 25517Ammonium Chloride용매

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온도
100 °C

실험 절차

A mixture of 4-methylphenol (30.0 g), 1,4-dibromobenzene (54.5 g), copper (I) iodide (4.40 g), potassium carbonate (5.11 g) and N,N-dimethylglycine (2.86 g) in DMF (300 mL) was stirred at 100° C. under N2 for 18 hr. The mixture was diluted with sat. NH4Cl aq. at 0° C. and extracted with EtOAc. The organic layer was separated, washed with sat. NH4Cl aq., 1N NaOH aq. and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography (silica gel, eluted with hexane) to give the title compound (39.5 g) as a colorless solid.

후처리

  1. extractionextracted with EtOAc
  2. customThe organic layer was separated
  3. washwashed with sat. NH4Cl aq., 1N NaOH aq. and brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by column chromatography (silica gel, eluted with hexane)

출처 및 근거

ORD 기록
ord-f9e2fc420efd45c481ca96ac2ccf6875
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08778934B2

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