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Sodium Methoxide → HCID 22494610, 화합물

HRID 1816686
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HRID 1816686 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14]Br)=[CH:4][CH:3]=1.[CH3:16][O-:17].[Na+]>CO>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][O:17][CH3:16])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 224947501-Bromo-4-((6-bromohexyl)oxy)benzene

생성물 1

HCID 22494610HCID 22494610, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

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온도
70 °C

실험 절차

A mixture of 1-bromo-4-(6-bromohexyloxy)benzene (6.0 g) and sodium methylate (28% in methanol) (10.3 ml) in methanol (30 ml) was stirred for 2 hours at 70° C. (bath temp.), and then the solvent was evaporated. The residue was neutralized by 1N-hydrochloric acid and extracted with ethyl acetate (100 ml), and washed with water and brine. The organic layer was dried over magnesium sulfate. Magnesium sulfate was filtered off, and the filtrate was evaporated under reduced pressure to give a crude product. The crude product was purified by silica gel chromatography (20:1-10:1 hexane-ethyl acetate) to give 1-bromo-4-(6-methoxyhexyloxy)benzene (15.61 g) as a colorless oil.

후처리

  1. customthe solvent was evaporated
  2. extractionextracted with ethyl acetate (100 ml)
  3. washwashed with water and brine
  4. dry with materialThe organic layer was dried over magnesium sulfate
  5. filtrationMagnesium sulfate was filtered off
  6. customthe filtrate was evaporated under reduced pressure
  7. customto give a crude product
  8. customThe crude product was purified by silica gel chromatography (20:1-10:1 hexane-ethyl acetate)

출처 및 근거

ORD 기록
ord-8409838ccddf4daba9392066aa636ba2
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06884868B1

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