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Water → 3-Chlorobenzocyclobutene-1-carboxylic acid

HRID 2372757
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HRID 2372757 반응식
[Cl:1][C:2]1[C:9]2[CH2:8][CH:7]([C:10]#N)[C:6]=2[CH:5]=[CH:4][CH:3]=1.[OH-:12].[K+].[OH2:14]>C(O)C>[Cl:1][C:2]1[C:9]2[CH:8]=[C:7]([C:10]([OH:14])=[O:12])[C:6]=2[CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

HCID 198863753-Chlorobenzocyclobutene-1-carboxylic acid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

5.0 g of 3-chloro-1-cyanobenzocyclobutane (prepared according to the process described in Patent EP 119,107) are added to a solution of 6.0 g of potassium hydroxide in 58 ml of ethanol. The mixture is stirred at room temperature overnight. 7.5 ml of water are then added and the mixture is heated to reflux for 6 hours. The ethanol is evaporated off to dryness. The residue is taken up with water and the aqueous phase is washed with ethyl ether, then acidified (pH 1) with 1N hydrochloric acid and extracted with dichloromethane. The organic phase is dried, filtered and evaporated to dryness.

후처리

  1. temperaturethe mixture is heated
  2. temperatureto reflux for 6 hours
  3. customThe ethanol is evaporated off to dryness
  4. washthe aqueous phase is washed with ethyl ether
  5. extractionextracted with dichloromethane
  6. customThe organic phase is dried
  7. filtrationfiltered
  8. customevaporated to dryness

출처 및 근거

ORD 기록
ord-ac3c7d82db414898ab0a0bf7efd04f48
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05100902

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