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HRID 3100Erstellt: 24. Oktober 2026
Dimethyl acetylenedicarboxylate → HCID 178418477, Verbindung
https://huagongshe.com/de/reaction/3100
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl acetylenedicarboxylate | HCID 12980 | — |
| Edukt | Methyl 4-chloroanthranilate | HCID 80001 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | HCID 178418477 | HCID 178418477 | 28,9% |
Reaktionsschritte
A stirred mixture of methyl 2-amino-4-chlorobenzoate (2.50 g, 13.5 mM) and dimethyl acetylenedicarboxylate (2.05 g, 14.4 mM) in t-butanol (22 mL) was refluxed for 7 hr under a nitrogen atmosphere. After adding additional dimethyl acetylenedicarboxylate (1.16 g, 8.13 mM) and refluxing another 2.5 hr, the reaction mixture was allowed to cool to room temperature and potassium t-butoxide (1.56 g, 13.9 mM) was added in one portion. A precipitate formed and the resulting mixture was refluxed for 1.5 hr. The mixture was cooled to room temperature and filtered to separate the solids, which were washed with t-butanol and ether. The solids were dissolved in water and acidified with 1N sulfuric acid to form a precipitate. The resulting mixture was extracted with methylene chloride and the combined extracts were washed with brine and water, dried (MgSO4), filtered and concentrated to give a green solid. Recrystallization of this material from methanol provided dimethyl 7-chloro-4-hydroxyquinoline-2,3-dicarboxylate (1.15 g, 28.9%) as an off-white solid, mp 232-233° C.; MS(CI): 296 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05733910 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-d09058163d114c2aaa3e06a2b0426827 |
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| Quellennotiz | uspto-grants-1998_03 |
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