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2-Methoxyethanol → Methoxyethoxy-(3e)-1,3-pentadiene

HRID 991253
ノート
印刷プレビュー

反応式

HRID 991253 の反応式
[Na].Br[CH2:3]/[CH:4]=[CH:5]/[CH:6]=[CH2:7].[CH3:8][O:9][CH2:10][CH2:11][OH:12]>>[CH3:8][O:9][CH2:10][CH2:11][O:12][CH:7]=[CH:6]/[CH:5]=[CH:4]/[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 80192-MethoxyethanolHCID 5360545SodiumHCID 5365559(3E)-5-Bromo-1,3-pentadiene

生成物 1

HCID 131723540Methoxyethoxy-(3e)-1,3-pentadiene収率 75%

実験手順

Under a nitrogen atmosphere, to a stirred solution of sodium (0.53 g, 23 mmol) in 2-methoxyethanol (50 mL) at room temperature was added 5-bromo-(3E)-1,3-pentadiene (3.38 g, 23 mmol). The mixture was stirred overnight and then refluxed for three more hours. Excess 2-methoxyethanol was removed by distillation. Water was added to the cooled reaction mixture, which was then extracted with diethyl ether. The diethyl ether solution was dried over MgSO4, then stripped off at reduced pressure. Distillation at 87-88° C., 31 mmHg (water aspirator) yielded 2.46 g (75%) of the desired compound.

後処理

  1. temperaturerefluxed for three more hours
  2. customExcess 2-methoxyethanol was removed by distillation
  3. additionWater was added to the cooled reaction mixture, which
  4. extractionwas then extracted with diethyl ether
  5. dry with materialThe diethyl ether solution was dried over MgSO4
  6. distillationDistillation at 87-88° C.

出典と根拠

ORDレコード
ord-6e059a2bf50c41c48ba8f2be35d870b1
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06462207B1

反応ノート

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