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Hydrochloric Acid → Methyl 2,4,5-trimethylphenylacetate

HRID 1635904
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HRID 1635904 반응식
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([CH3:9])=[CH:4][C:3]=1[CH2:10][C:11]([OH:13])=[O:12].Cl.[CH3:15]O>>[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([CH3:9])=[CH:4][C:3]=1[CH2:10][C:11]([O:13][CH3:15])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 2989242-(2,4,5-Trimethylphenyl)acetic acid

생성물 1

HCID 22336857Methyl 2,4,5-trimethylphenylacetate

실험 절차

100 g (0.56 mol) of 2,4,5-trimethylphenylacetic acid were dissolved in 230 ml of methanol, 6 ml of concentrated hydrochloric acid were added and the mixture was heated under reflux for 10 hours. It was then cooled to room temperature and the methanol was removed in vacuo. The residue was stirred into a solution of 53 g of sodium carbonate, dissolved in 260 ml of water, and the organic phase was taken up in 200 ml of toluene. The organic phase was separated off, dried and concentrated and the residue was distilled. 48.6 g of methyl 2,4,5-trimethylphenylacetate having a boiling point of 86° C. under 0.2 mbar were obtained.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
temperature
the mixture was heated
  • temperatureunder reflux for 10 hours
  • customthe methanol was removed in vacuo
  • dissolutiondissolved in 260 ml of water
  • customThe organic phase was separated off
  • customdried
  • concentrationconcentrated
  • distillationthe residue was distilled
  • 출처 및 근거

    ORD 기록
    ord-225f6a712526409195885c165ac4f6b0
    출처 데이터셋
    uspto-grants-2003_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06511942B1

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