Reaktion #69278

ord-7514952082aa4690a649a793d88fb62a

Reaktionsgleichung

Cl
HCl
O=C(O)CC(=O)O
malonic acid
C1CCNCC1
piperidine
O=CC1CCCC1
cyclopentanecarbaldehyde
O=C(O)/C=C/C1CCCC1
product
Ausbeute 77.0%
O=C(O)/C=C/C1CCCC1
(2E)-3-Cyclopentylacrylic acid
Ausbeute 77.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
40°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was then cooled in an ice bath
  2. 2
    ExtraktionThe product was extracted with ether
  3. 3
    ExtraktionThe ether extract
  4. 4
    Waschenwas washed with aq. HCl and brine
  5. 5
    Trocknendried over sodium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    Sonstigethe solvent was removed in vacuo

Vorschrift

To a solution of malonic acid (1.06 g, 10.2 mol) in pyridine (1.25 mL) was added piperidine (0.15 mL) and cyclopentanecarbaldehyde (1.00 g, 10.2 mmol). The mixture was heated to 40° C. for 2 hours, followed by stirring at room temperature for 16 hours. The mixture was then cooled in an ice bath and 2N HCl was added to acidify. The product was extracted with ether. The ether extract was washed with aq. HCl and brine, dried over sodium sulfate, filtered, and the solvent was removed in vacuo to afford the product (1.30 g, 77%), which was used without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530485B2uspto-grants-2013_09