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Acetylene → 1-Bromo-trans-1-octen-3-one

HRID 67008
ノート
印刷プレビュー

反応式

HRID 67008 の反応式
[Br-].[Al+3].[Br-].[Br-].[Br:5][CH2:6][CH2:7]Br.C#C.[C:11](Br)(=[O:17])[CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]>[Cl-].[Na+].O>[Br:5]/[CH:6]=[CH:7]/[C:11](=[O:17])[CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6326Acetylene2 回HCID 78391,2-DibromoethaneHCID 166749BromhydrolHCID 13226800Hexanoyl bromide

生成物 1

HCID 117903381-Bromo-trans-1-octen-3-one

試薬・触媒・溶媒 1

HCID 57417360Sodium chloride; water溶媒

実験手順

A mixture of 300 g. of aluminum bromide and 250 ml. of 1,2-dibromoethane, cooled in an ice bath and protected from moisture, is saturated with acetylene. To the mixture is added with ice cooling 150 g. of hexanoyl bromide (Example 991) over a period of 20 minutes and the resulting mixture is treated with acetylene until gas uptake ceases. The reaction mixture is poured onto 500 ml. of saturated brine and 500 g. of ice. The resulting mixture is extracted twice with 500 ml. of ether. The combined organic extracts are washed twice with 500 ml. of saturated brine and dried with anhydrous sodium sulfate. To the organic phase is added 5 g. of hydroquinone and the solvent is evaporated in vacuo to yield the crude 1-bromo-trans-1-octen-3-one.

後処理

  1. additionA mixture of 300 g
  2. additionThe reaction mixture is poured onto 500 ml
  3. extractionThe resulting mixture is extracted twice with 500 ml
  4. washThe combined organic extracts are washed twice with 500 ml
  5. dry with materialof saturated brine and dried with anhydrous sodium sulfate
  6. additionTo the organic phase is added 5 g
  7. customof hydroquinone and the solvent is evaporated in vacuo

出典と根拠

ORDレコード
ord-3570da56e8dc4f0faa4be69de5640b85
出典データセット
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04343949

反応ノート

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