HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 647902Erstellt: 25. Oktober 2026
Hydrochloric Acid → Ethyl 5-(2-formyl-3-hydroxy-4-methoxycarbonylphenoxy)pentanoate
https://huagongshe.com/reaction/647902
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Ethyl 5-bromovalerate | HCID 84580 | — |
| Edukt | Methyl 2,4-dihydroxy-3-formylbenzoate | HCID 4413713 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Ethyl 5-(2-formyl-3-hydroxy-4-methoxycarbonylphenoxy)pentanoate | HCID 20484347 | 42% |
Reaktionsschritte
Methyl 2,4-dihydroxy-3-formylbenzoate (10.0 g, 0.051 M) was added to dimethylformamide (100 ml), then to this mixture was added sodium hydride (1.344 g, 0.056 M), portionwise. The mixture became warm and effervescence occurred. When the addition was complete the reaction mixture was left to stir at room temperature for 10 minutes. To this solution was then added sodium iodide (0.765 g), ethyl 5-bromovalerate (11.7 g, 0.056 M), and a further 20 ml of dimethylformamide. The whole was brought to 60° C. and left to stir for 5 days. The reaction mixture was cooled, poured into water (200 ml), acidified with concentrated hydrochloric acid, and extracted into ethyl acetate (2×75 ml). The combined organic layers were washed with water (2×75 ml), 5% sodium hydroxide solution (50 ml), water (50 ml) and brine (50 ml), dried (magnesium sulphate), filtered and the solvent removed in vacuo to give ethyl 5-(2-formyl-3-hydroxy-4-methoxycarbonylphenoxy)pentanoate 6.92 g, 42% as a yellow oil, purified by column chromatography and obtained as a pale-yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04410537 |
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| Quelldatensatz | uspto-grants-1983_10 |
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| ORD ID | ord-547556c0c1344c01adf5f7a7d54a07e2 |
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| Quellennotiz | uspto-grants-1983_10 |
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