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Dimethylformamide → 4-methacryloyloxybutyl (E)-3-(4-ethoxycarbonyloxyphenyl)acrylate

HRID 1637133
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1637133
[CH2:1]([O:3][C:4]([O:6][C:7]1[CH:17]=[CH:16][C:10](/[CH:11]=[CH:12]/[C:13]([OH:15])=[O:14])=[CH:9][CH:8]=1)=[O:5])[CH3:2].CN(C)[CH:20]=[O:21]>S(Cl)(Cl)=O>[CH2:1]([O:3][C:4]([O:6][C:7]1[CH:17]=[CH:16][C:10](/[CH:11]=[CH:12]/[C:13]([O:15][CH2:10][CH2:9][CH2:8][CH2:7][O:6][C:20](=[O:21])[C:12]([CH3:13])=[CH2:11])=[O:14])=[CH:9][CH:8]=1)=[O:5])[CH3:2]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 6228DimethylformamideHCID 12876666(2E)-3-{4-[(ethoxycarbonyl)oxy]phenyl}prop-2-enoic acid

Produkt 1

HCID 220777024-methacryloyloxybutyl (E)-3-(4-ethoxycarbonyloxyphenyl)acrylate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 24386Thionyl ChlorideLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution of 5.2 g of 4-(E)-ethyloxycarbonyloxycinnamic acid in 20 ml of thionyl chloride and 0.05 ml of N,N-dimethylformamide was heated under reflux for 3 hours. Subsequently, excess thionyl chloride was distilled off. 3.3 g of 4-hydroxybutyl methacrylate were added dropwise to a solution of the resulting 4-(E)-ethyloxycarbonyloxycinnamoyl chloride in 15 ml of pyridine while stirring at 0° C. within 15 minutes. The reaction mixture was stirred at room temperature for a further 12 hours, then poured into water and extracted three times with 50 ml of ethyl acetate each time. The combined organic phases were dried over magnesium sulphate, filtered and subsequently concentrated. Chromatographic purification on silica gel with hexane/ethyl acetate (vol. 7:3) gave 3 g of 4-methacryloyloxybutyl (E)-3-(4-ethoxycarbonyloxyphenyl)acrylate, m.p. 54°-56° C.

Aufarbeitung

  1. temperatureunder reflux for 3 hours
  2. distillationSubsequently, excess thionyl chloride was distilled off
  3. addition3.3 g of 4-hydroxybutyl methacrylate were added dropwise to a solution of the resulting 4-(E)-ethyloxycarbonyloxycinnamoyl chloride in 15 ml of pyridine
  4. stirringThe reaction mixture was stirred at room temperature for a further 12 hours
  5. additionpoured into water
  6. extractionextracted three times with 50 ml of ethyl acetate each time
  7. dry with materialThe combined organic phases were dried over magnesium sulphate
  8. filtrationfiltered
  9. concentrationsubsequently concentrated
  10. customChromatographic purification on silica gel with hexane/ethyl acetate (vol. 7:3)

Quellen und Nachweise

ORD-Eintrag
ord-35df1e4e10354492bf662be6aad488f4
Quelldatensatz
uspto-grants-2000_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
USRE036625

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