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Water → 2-Chlorobicyclo(4.2.0)octa-1(6),2,4-triene-7-carboxylic acid

HRID 1026625
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HRID 1026625 반응식
[Cl:1][C:2]1[C:7]2[CH2:8][CH:9]([C:10]#N)[C:6]=2[CH:5]=[CH:4][CH:3]=1.[OH-:12].[K+].[OH2:14]>CCO>[Cl:1][C:2]1[C:7]2[CH2:8][CH:9]([C:10]([OH:14])=[O:12])[C:6]=2[CH:5]=[CH:4][CH:3]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 14797Potassium HydroxideHCID 135607112-Chlorobicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile

생성물 1

HCID 102617682-Chlorobicyclo(4.2.0)octa-1(6),2,4-triene-7-carboxylic acid수율 85%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 3-chloro-1,2-dihydrocyclobutabenzene-1-carbonitrile (196 mmol, 32 g) and potassium hydroxide (978 mmol, 54.9 g) in EtOH (500 ml)/water (100 ml) was stirred at reflux for 2 h. After evaporation of the organic solvent, the aqueous residue was washed with Et2O. The organic layer was extracted with 2N NaOH aq. and combined aqueous layers were acidified with 5 N HCl and extracted with Et2O. The extracts were washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was washed with heptane/Et2O (5/1) to afford 3-chloro-1,2-dihydrocyclobutabenzene-1-carboxylic acid (85% yield, 30.3 g).

후처리

  1. temperatureat reflux for 2 h
  2. customAfter evaporation of the organic solvent
  3. washthe aqueous residue was washed with Et2O
  4. extractionThe organic layer was extracted with 2N NaOH aq. and combined aqueous layers
  5. extractionextracted with Et2O
  6. washThe extracts were washed with brine
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated in vacuo
  9. washThe residue was washed with heptane/Et2O (5/1)

출처 및 근거

ORD 기록
ord-e6447b9dbd21416fb32fc10f838abec5
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08729274B2

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