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Hydrogen Bromide → 1-Bromocyclopentane-1-carboxylic acid

HRID 1075760
ノート
印刷プレビュー

反応式

HRID 1075760 の反応式
[C:1]1([C:6]([OH:8])=[O:7])[CH2:5][CH2:4][CH2:3][CH:2]=1.[Br:9]Br.Br>O>[Br:9][C:1]1([C:6]([OH:8])=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]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

5

反応物 3

HCID 260Hydrogen BromideHCID 24408BromineHCID 959641-Cyclopentene-1-carboxylic acid

生成物 1

HCID 134118411-Bromocyclopentane-1-carboxylic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
60 °C

実験手順

20 g (0.176 mol) of cyclopentaencarboxylic acid are mixed with red phosphorus (2.5 g). 17.9 ml (0.352 mol) of bromine are added dropwise thereto over the course of 2 hours; thereupon, a vigorous reaction is observed, with liberation of hydrogen bromide. The reaction contents are then stirred for 3 hours at 60°C. The oil, which shows a heavy dark coloration, is cooled and poured into water and the resulting reaction mixture is extracted three times with ether. The collected ether phases are washed with water and dried. After distilling off the ether, the oily residue is distilled in a high vacuum.

後処理

  1. customover the course of 2 hours
  2. customthereupon, a vigorous reaction
  3. customThe reaction contents
  4. temperatureis cooled
  5. customthe resulting reaction mixture
  6. extractionis extracted three times with ether
  7. washThe collected ether phases are washed with water
  8. customdried
  9. distillationAfter distilling off the ether
  10. distillationthe oily residue is distilled in a high vacuum

出典と根拠

ORDレコード
ord-654a526be28a4576b8180e27880c6919
出典データセット
uspto-grants-1976_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03954730

反応ノート

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