HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 969475Erstellt: 25. Oktober 2026
Tetrahydrofuran → Methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate
https://huagongshe.com/reaction/969475
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| Edukt | Methyl 6-hydroxy-2-naphthoate | HCID 390995 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate | HCID 12085484 | 85% |
Reaktionsschritte
3.3 g (83 mmol) of 60% sodium hydride in oil are added portionwise to a solution of 14 g (69 mmol) of methyl 6-hydroxynaphthalene-2-carboxylate in 180 ml of an equivolume mixture of tetrahydrofuran and dimethylformamide. After the evolution of gas has ceased, 8.7 ml (76 mmol) of methoxyethoxymethyl chloride are added dropwise. The reaction medium is stirred at room temperature for 3 hours, immersed into ice-cold water and extracted with ethyl ether. The organic phase is dried over sodium sulfate, filtered and concentrated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture. 17 g of methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate are obtained in the form of a colorless oil, in a yield of 85%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07307078B2 |
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| Quelldatensatz | uspto-grants-2007_12 |
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| ORD ID | ord-46d1260935e44f699670d3851c25d14e |
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| Quellennotiz | uspto-grants-2007_12 |
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