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

HRID 971864
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HRID 971864 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 53942620HCID 53942620, 화합물

생성물 1

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

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

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.).

후처리

  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

출처 및 근거

ORD 기록
ord-c243ccd4942943939d5b886bce7bfe8f
출처 데이터셋
uspto-grants-1979_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04161538

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