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HRID 27577作成日:2026年10月26日

Acetaldehyde → (-)-Carnitine

https://huagongshe.com/reaction/27577

反応式

関与物質

役割名称HCID仕込み量
反応物AcetaldehydeHCID 177—
反応物NadhHCID 439153—
反応物(3-Carboxy-2-oxopropyl)trimethylammonium chlorideHCID 2724491—
溶媒Acetic AcidHCID 176—
生成物(-)-CarnitineHCID 1091777.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04221869
出典データセットuspto-grants-1980_09
ORD IDord-69843a9b4f804ce7a10f54a4d2af355d
出典メモuspto-grants-1980_09