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Hexane → 2-Bromo-1,3-dimethoxybenzene

HRID 54025
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인쇄 미리보기

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HRID 54025 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[CH:4]=1.C([Li])CCC.CCCCCC.C(Br)(Br)(Br)[Br:23]>C(OCC)C.C(OCC)(=O)C.O>[Br:23][C:4]1[C:3]([O:2][CH3:1])=[CH:8][CH:7]=[CH:6][C:5]=1[O:9][CH3:10]
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참가 물질

8

반응물 4

HCID 8058HexaneHCID 90251,3-DimethoxybenzeneHCID 11205Carbon tetrabromideHCID 178418339Butyllithium

생성물 1

HCID 6122962-Bromo-1,3-dimethoxybenzene수율 57.3%

시약·촉매·용매 3

HCID 962Water용매
HCID 3283
Diethyl Ether
용매
2회
HCID 8857Ethyl Acetate용매

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온도
0 °C

실험 절차

In a solution of 1,3-dimethoxybenzene (3.0 g, 21.7 mmol) dissolved in diethyl ether (90 ml), a 1.65M solution of n-butyl lithium in n-hexane (19.8 ml, 32.7 mmol of n-butyl lithium) was added at room temperature, and a reaction mixture was heated to reflux for 4 hours. After cooling the reaction mixture to 0° C., a solution of carbon tetrabromide (15.8 g, 47.7 mmol) in diethyl ether (60 ml) was added to the mixture, and stirred at room temperature for 20 hours. A small amount of water was added to the reaction mixture, and then the reaction mixture was diluted with ethyl acetate (90 ml). The organic layer was washed with water and dried over anhydrous magnesium sulfate. Thereafter, the solvent was evaporated off, and the residue was purified by column chromatography to obtain 1-bromo-2,6-dimethoxybenzene (2.70 g).

후처리

  1. temperaturea reaction mixture was heated
  2. temperatureto reflux for 4 hours
  3. washThe organic layer was washed with water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customThereafter, the solvent was evaporated off
  6. customthe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-fc9b38681b0e43a0aaebc84a04652613
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05621129

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