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Ethanol → Ethyl 4-chlorocinnamate

HRID 2242563
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2242563
[Cl:1][C:2]1[CH:12]=[CH:11][C:5](/[CH:6]=[CH:7]/[C:8]([OH:10])=[O:9])=[CH:4][CH:3]=1.[CH2:13](O)[CH3:14]>S(=O)(=O)(O)O>[CH2:13]([O:9][C:8](=[O:10])/[CH:7]=[CH:6]/[C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:12][CH:11]=1)[CH3:14]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 702EthanolHCID 6377974-Chlorocinnamic acid

Produkt 1

HCID 5373977Ethyl 4-chlorocinnamate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1118Sulfuric AcidKatalysator

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

To a solution of trans-4-chlorocinnamic acid (10 g, 55 mmol) in ethanol (60 mL) was added a catalytic amount of concentrated sulfuric acid (2-3 drops), and the mixture was heated (70° C.) until a majority of the starting material was consumed as evidenced by LCMS. The reaction mixture was concentrated and the contents were redissolved in ethyl acetate. The organic phase was extracted with an aqueous solution of sodium bicarbonate (5%, 3×) followed by a brine wash. The organic phase was dried (MgSO4), filtered and concentrated to afford trans-4-chlorocinnamic acid ethyl ester as a colorless oil. MS (ESI) m/z 211.1 ([M+H]+).

Aufarbeitung

  1. customwas consumed
  2. concentrationThe reaction mixture was concentrated
  3. dissolutionthe contents were redissolved in ethyl acetate
  4. extractionThe organic phase was extracted with an aqueous solution of sodium bicarbonate (5%, 3×)
  5. washwash
  6. dry with materialThe organic phase was dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-5949ce4d83b64e6fb60d0164602020de
Quelldatensatz
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07671238B2

Notizen zur Reaktion

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