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Potassium Hydroxide → 2-(2,5-Dimethylphenyl)-2-hydroxyacetic acid

HRID 55565
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HRID 55565 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[C:9]([OH:20])(C(OCC)=O)[C:10]([O:12]CC)=[O:11].[OH-].[K+]>O>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[CH:9]([OH:20])[C:10]([OH:12])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 12836549Diethyl 2-(2,5-dimethylphenyl)-2-hydroxymalonate

생성물 1

HCID 2776622-(2,5-Dimethylphenyl)-2-hydroxyacetic acid

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A sample of the diethyl (2,5-dimethylphenyl)-hydroxymalonate (21 parts) was reacted with a solution of potassium hydroxide (21 parts) in water (84 parts) at 98° C. for 5 hours. After cooling to ambient temperature, the reaction was washed with diethyl ether and acidified with 10M hydrochloric acid. After heating to 98° C. for a further 2 hours, the cooled materials was extracted into diethyl ether. The separated organic phase was dried over magnesium sulfate, filtered and the solvent was evaporated under reduced pressure. The crude amber coloured oil (15 parts) solidified on standing. Recrystallisation from toluene gave 2,5-dimethylmandelic acid (7 parts). The 1Hnmr, 13Cnmr and mass spectra were all consistent with the structure.

후처리

  1. washthe reaction was washed with diethyl ether
  2. temperatureAfter heating to 98° C. for a further 2 hours
  3. extractionthe cooled materials was extracted into diethyl ether
  4. dry with materialThe separated organic phase was dried over magnesium sulfate
  5. filtrationfiltered
  6. customthe solvent was evaporated under reduced pressure
  7. customRecrystallisation from toluene

출처 및 근거

ORD 기록
ord-dd88efefd2d74ea4b0fe4b474d5093ee
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05625080

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