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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27576Erstellt: 23. Oktober 2026

Acetic Acid → DL-Carnitine

https://huagongshe.com/de/reaction/27576

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktEthanolHCID 702—
EduktNadhHCID 439153—
ProduktDL-CarnitineHCID 288—
ProduktNadhHCID 439153—

Reaktionsschritte

Carnitine was synthesized as in example 2, except that the NADH regeneration system comprised, in addition to alcohol dehydrogenase, aldehyde dehydrogenase (E.C. 1.2.1.5) which oxidizes the aldehyde (formed by action of alcohol dehydrogenase on ethanol) to acetic acid. Two molecules of NADH were formed from one molecule of ethanol (instead of one in the preceeding example) and the reaction balance was strongly displaced in favour of NADH and acetic acid formation. It was thus no longer necessary to eliminate acetaldehyde as in the preceeding example. The conditions were thus those of example 2, except that 125 units of purified aldehyde dehydrogenase (Boehringer ref. 171.832) were added to the reaction medium and nitrogen bubbling was omitted. After 24 hours, 0.764 g of L-carnitine was formed with a yield of 77.5% with respect to dehydrocarnitine hydrochloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04221869
Quelldatensatzuspto-grants-1980_09
ORD IDord-49b8a2a428ac4d3c9d9320983dae0121
Quellennotizuspto-grants-1980_09