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llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
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Carbon Dioxide → 2-Methylglutaric Acid

HRID 359959
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 359959
[C:1](=[O:3])=[O:2].C([CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12]C)=[O:11])=O.C(OC)(=O)CCCCC([O-])=O>>[CH3:6][CH:7]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])[C:1]([OH:3])=[O:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 280Carbon DioxideHCID 81164Methyl 6-oxohexanoateHCID 6994472Methyl adipate

Produkt 1

HCID 120462-Methylglutaric AcidAusbeute 96 %

Versuchsvorschrift

The cleavage in stage (c) is advantageously carried out in the presence of molecular oxygen or a gas which contains molecular oxygen and an inert gas, such as nitrogen, carbon dioxide, argon or steam. A molar ratio of formylvaleric esters to molecular oxygen of from 1:0.05 to 1:3, in particular from 1:0.2 to 1:1.5, e.g., from 1:0.25 to 1:1.25, is advantageously used. This increases the catalyst life and in particular the yield of pentenoic esters. The presence of molecular oxygen was not indicated since methyl 5-formylvalerate is oxidized to monomethyl adipate in a yield of 96% by molecular oxygen at as low as 50° C., as disclosed in European Patent 131,860, and it was therefore to be expected that 4- and 3-formylvaleric esters would be oxidized in a similar manner to give 2-methylglutaric acid and 3-ethylsuccinic esters.

Aufarbeitung

  1. temperatureThis increases the catalyst life

Quellen und Nachweise

ORD-Eintrag
ord-b40f2f7ca4574b5c9d20c335587813c3
Quelldatensatz
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05003102

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