HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1649946Erstellt: 25. Oktober 2026
Hydrochloric Acid → L-homoalanin-4-yl(methyl)phosphinic acid hydrochloride
https://huagongshe.com/reaction/1649946
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Methanol | HCID 887 | — |
| Edukt | HCID 178474815 | HCID 178474815 | — |
| Produkt | Hydrochloric Acid | HCID 313 | — |
| Produkt | L-homoalanin-4-yl(methyl)phosphinic acid hydrochloride | HCID 12701464 | 91,9% |
Reaktionsschritte
0.0087 g (0.019 mmol) of chloronorbornadienerhodium(I) dimer and 0.022 g (0.053 mmol) of the compound Va are dissolved in 5 ml of methanol under an atmosphere of argon. The catalyst solution obtained is added under argon to a solution of 2.21 g (0.01 mol) of 2-acetamido-4-(hydroxymethylphosphinyl)-2-butenoic acid in 45 ml of methanol. The reaction vessel is evacuated, then hydrogenation is performed at a pressure of 3.0 bar. After a reaction time of 44 hours, the reaction vessel is depressurized, the reaction mixture evaporated down, the residue taken up in water and the precipitated catalyst separated off. As a result of adding an equivalent quantity of concentrated hydrochloric acid to the filtrate, a 6N hydrochloric acid solution is prepared which is boiled under reflux for 12 hours. After evaporating this solution down, 2.0 g (91.9% of theory) of L-homoalanin-4-yl(methyl)phosphinic acid hydrochloride is obtained as a white solid which is purified by recrystallization from an ethanol/water mixture.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04922006 |
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| Quelldatensatz | uspto-grants-1990_05 |
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| ORD ID | ord-3b5954c9604849f1b2b973f418798d61 |
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| Quellennotiz | uspto-grants-1990_05 |
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