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Hydrochloric Acid → Methyl 2,4,5-trimethylphenylacetate

HRID 585469
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 585469
[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]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

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

Produkt 1

HCID 22336857Methyl 2,4,5-trimethylphenylacetate

Versuchsvorschrift

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. Dimethyl 2-(2,4,5-trimethylphenyl)-malonate

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 10 hours
  3. customthe methanol was removed in vacuo
  4. dissolutiondissolved in 260 ml of water
  5. customThe organic phase was separated off
  6. customdried
  7. concentrationconcentrated
  8. distillationthe residue was distilled

Quellen und Nachweise

ORD-Eintrag
ord-b3309ba223e3458d8bc0bc7e22ea38be
Quelldatensatz
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06933261B2

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