참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetaldehyde | HCID 177 | — |
| 반응물 | Nadh | HCID 439153 | — |
| 반응물 | (3-Carboxy-2-oxopropyl)trimethylammonium chloride | HCID 2724491 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | (-)-Carnitine | HCID 10917 | 77.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04221869 |
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| 출처 데이터셋 | uspto-grants-1980_09 |
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| ORD ID | ord-69843a9b4f804ce7a10f54a4d2af355d |
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| 출처 메모 | uspto-grants-1980_09 |
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