HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435479Generated: October 26, 2026
Chloride → N-acetyl glutamyl carnitine hydrochloride
https://huagongshe.com/reaction/435479
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | N-acetyl-L-glutamic acid | HCID 70914 | — |
| Reactant | 3-Hydroxy-4-(trimethylammonio)butanoate hydrochloride | HCID 9794197 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | N-acetyl glutamyl carnitine hydrochloride | HCID 131713077 | — |
Reaction Steps
4.2 g (0.021 moles) of carnitine hydrochloride are dissolved in 12 mls of trifluoroacetic acid, then at 35° C. and under vigorous stirring 20 cc of a solution of anhydrous chloroform wherein about 4.36 g (0.021 moles) of the acide chloride of the N-acetyl glutamic acid have been dissolved are added dropwise. The reaction is allowed to proceed for about 14 hours at 35° C., and subsequently at 50° C. for two further hours. The reaction mixture is cooled. Upon acetone addition (40 mls) no precipitate forms even though the mixture is cooled below 0° C. 140 mls of ethyl ether are added and after keeping the mixture at 8° C. overnight there are obtained 6.2 g of a solid white product which is crystallized with ethyl ether. After 2 crystallizations 5.4 g (68%) of the desired product having the following characteristics are obtained:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04401827 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-542c67c985bb42a79898f9ca484a9e7b |
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| Source note | uspto-grants-1983_08 |
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