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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27577생성일: 2026년 10월 25일

Acetaldehyde → (-)-Carnitine

https://huagongshe.com/reaction/27577

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물NadhHCID 439153—
반응물(3-Carboxy-2-oxopropyl)trimethylammonium chlorideHCID 2724491—
용매Acetic AcidHCID 176—
생성물(-)-CarnitineHCID 1091777.5%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04221869
출처 데이터셋uspto-grants-1980_09
ORD IDord-69843a9b4f804ce7a10f54a4d2af355d
출처 메모uspto-grants-1980_09