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Sodium Methoxide → HCID 22494610、化合物

HRID 1816686
ノート
印刷プレビュー

反応式

HRID 1816686 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 22494610HCID 22494610、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
70 °C

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-8409838ccddf4daba9392066aa636ba2
出典データセット
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06884868B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート