HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 478947Erstellt: 24. Oktober 2026
Hydrochloric Acid → (3S)-6,7-Dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
https://huagongshe.com/de/reaction/478947
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Levodopa | HCID 6047 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Formaldehyde--water (1/1) | HCID 22136924 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | (3S)-6,7-Dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid | HCID 12926159 | 95,4% |
Reaktionsschritte
To a cold (0-5° C.) suspension of Levodopa (197.2 g, 1.0 mol) in water (1.18 L) was added 32% aqueous HCl (159.5 g, 1.4 mol). The resulting solution was cooled to 0-5° C., and 37% formaldehyde water solution (243.24 g, 3.0 mol) was added. The resulting solution was allowed to warm to 20-25° C., and stirred at 20-25° C. for 10 h. The reaction solution was cooled to 0-5° C., and 2 N aqueous NaOH (700 mL, 1.4 mol) was slowly added to adjust pH to 5-5.5. White or light yellow solids precipitated during the addition. The resulting suspension was stirred at 0-5° C. for 2-3 h. The mixture was filtered, and rinsed with water (2×500 mL). The solids were dried under vacuum to give 199.52 g of a light yellow solid. Yield=95.3%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06642384B1 |
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| Quelldatensatz | uspto-grants-2003_11 |
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| ORD ID | ord-6ceb0d06cf6e43d39071939c1c56122e |
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| Quellennotiz | uspto-grants-2003_11 |
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