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Hydrogen Bromide → 4-[(2-Oxocyclopentyl)methyl]benzeneacetic acid

HRID 971864
ノート
印刷プレビュー

反応式

HRID 971864 の反応式
Br.C(OC([C:7]1([CH2:13][C:14]2[CH:19]=[CH:18][C:17]([CH2:20][C:21]([O:23]CC)=[O:22])=[CH:16][CH:15]=2)[CH2:11][CH2:10][CH2:9][C:8]1=[O:12])=O)C>O1CCOCC1>[O:12]=[C:8]1[CH2:9][CH2:10][CH2:11][CH:7]1[CH2:13][C:14]1[CH:15]=[CH:16][C:17]([CH2:20][C:21]([OH:23])=[O:22])=[CH:18][CH:19]=1
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 2

HCID 260Hydrogen BromideHCID 53942620HCID 53942620、化合物

生成物 1

HCID 199226184-[(2-Oxocyclopentyl)methyl]benzeneacetic acid収率 93.3%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

Into a mixture of 20 ml of 47% hydrobromic acid and 15 ml of dioxane was dissolved 9.2 g of ethyl 4-(1-ethoxycarbonyl-2-oxocyclopentan-1-ylmethyl)phenylacetate and the solution was refluxed for 6 hours. The solvent was then removed by distillation from the reaction mixture, the residue was poured into ice-water and extracted with ether. The extract was washed with water, dried over anhydrous sodium sulfate, the solvent removed by distillation to give an oily substance, which was subjected to a vacuum distillation to yield 6.0 g of an oily product, b.p. 185°-195° C. at 0.7 mm Hg (bath temp.).

後処理

  1. temperaturethe solution was refluxed for 6 hours
  2. customThe solvent was then removed by distillation from the reaction mixture
  3. additionthe residue was poured into ice-water
  4. extractionextracted with ether
  5. washThe extract was washed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. customthe solvent removed by distillation
  8. customto give an oily substance, which
  9. distillationwas subjected to a vacuum distillation

出典と根拠

ORDレコード
ord-c243ccd4942943939d5b886bce7bfe8f
出典データセット
uspto-grants-1979_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04161538

反応ノート

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