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Carbon Dioxide → 4-Acetylbutyric acid

HRID 1641602
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1641602
ON1[C:6](=O)[CH2:5][CH2:4][C:3]1=[O:8].[CH3:9]C1CCCC=1.[C:15](=[O:17])=[O:16].O=O>C(O)(=O)C.O.O.O.O.C([O-])(=O)C.[Co+2].C([O-])(=O)C>[O:8]=[C:3]([CH3:9])[CH2:4][CH2:5][CH2:6][C:15]([OH:17])=[O:16]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 280Carbon DioxideHCID 977OxygenHCID 127461-MethylcyclopenteneHCID 80170N-Hydroxysuccinimide

Produkt 1

HCID 184074-Acetylbutyric acidAusbeute 60 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 61372Cobalt(II) acetate tetrahydrate
Katalysator
HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

This reaction was performed with a solution of 0.1191 g (1.03 mmol) of N-hydroxysuccinimide, 2.0 g (24.3 mmol) of 1-methylcyclopentene and 0.1330 g (0.53 mmol) of cobalt acetate tetrahydrate in 40 ml of acetic acid was heated to 100° C. in a Parr Hastelloy reactor with temperature and pressure transducer. After the temperature reached 100° C., 745 psi of CO2 was introduced into the reactor, then 120 psi of O2 was added slowly to the reactor. The mixture was stirred under pressure for one hour at 100° C., then the pressure was released, and the mixture was cooled to room temperature. The solution was extracted with ethyl acetate then with a saturated NaCl solution in water and, dried over Na2SO4 to give, as the major 60% 5-ketohexanoic acid.

Aufarbeitung

  1. customreached 100° C.
  2. temperaturethe mixture was cooled to room temperature
  3. extractionThe solution was extracted with ethyl acetate
  4. dry with materialwith a saturated NaCl solution in water and, dried over Na2SO4

Quellen und Nachweise

ORD-Eintrag
ord-bb84a1387e05460f9070cd4786486e76
Quelldatensatz
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08115029B2

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