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Potassium Hydroxide → HCID 20304493, 화합물

HRID 328929
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HRID 328929 반응식
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([CH:10]2[O:20][CH:11]2[C:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[O:13])=[CH:6][CH:5]=1)([OH:3])=[O:2].[OH-].[K+]>C(O)C>[C:1]([C:4]1[CH:5]=[CH:6][C:7]([CH2:10][C:11](=[O:20])[C:12]([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)=[O:13])=[CH:8][CH:9]=1)([OH:3])=[O:2]
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참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 20304490HCID 20304490, 화합물

생성물 1

HCID 20304493HCID 20304493, 화합물수율 100%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

To a solution of 5.63 g of 3-(4-carboxyphenyl)-1-phenyl-2,3-epoxy-1-propanone in 100 ml of ethanol at 85°-90° C was added a solution of 6 g of potassium hydroxide in 100 ml of ethanol with stirring over 5 min. The reaction mixture was heated at 85°-90° C for 5 min. and then allowed to cool to room temperature. The solution was evaporated to dryness and the residue was dissolved in 300 ml of ice-water and acidified with 125 ml of hydrochloric acid. After stirring for 30 min., the precipitate was collected and washed with water. The precipitate was dissolved in 600 ml of ethyl acetate and the solution was dried and filtered. The filtrate was evaporated to give 5.63 g (100%) of 3-(4-carboxyphenyl)-1-phenyl-1,2-propanedione as a yellow solid.

후처리

  1. temperatureThe reaction mixture was heated at 85°-90° C for 5 min.
  2. customThe solution was evaporated to dryness
  3. dissolutionthe residue was dissolved in 300 ml of ice-water
  4. stirringAfter stirring for 30 min.
  5. customthe precipitate was collected
  6. washwashed with water
  7. dissolutionThe precipitate was dissolved in 600 ml of ethyl acetate
  8. customthe solution was dried
  9. filtrationfiltered
  10. customThe filtrate was evaporated

출처 및 근거

ORD 기록
ord-d719451415db4af0bdca169d47d6a4cb
출처 데이터셋
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04018884

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