HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 67056Erstellt: 23. Oktober 2026
Benzyl Alcohol → Benzyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride
https://huagongshe.com/de/reaction/67056
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzyl Alcohol | HCID 244 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid | HCID 95489 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Benzyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride | HCID 20273210 | — |
Reaktionsschritte
Benzyl alcohol, 750 ml, was treated with 150 g of commercial polyphosphoric acid and warmed and stirred at 90° C. to obtain a homogeneous mixture. Solid 1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid (S-form) 165.2 g was added. The mixture was stirred 4 hours at 95°-105° C. and then allowed to stand at room temperature for 18 hours. A solution of 18.5 g gaseous hydrochloric acid in 2.5 l of anhydrous ether was added, and the product separated slowly on cooling overnight. Filtration gave the crude benzyl 1,2,3,4-tetrahydro-3-isoquinoline carboxylate hydrochloride. This was purified by recrystallization from ethanol twice to give material with mp 190.5°-191° C.; [α]D 23=-83.3° (1% 1:1 methanol/1 N hydrochloric acid).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04344949 |
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| Quelldatensatz | uspto-grants-1982_08 |
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| ORD ID | ord-d41cb35c3c15423083594c06b142ee98 |
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| Quellennotiz | uspto-grants-1982_08 |
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