HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1679530Erstellt: 25. Oktober 2026
Water → 2,2-dimethyl-7-(2-dimethylaminoethoxy)-4(6-methoxy-2-naphthyl)-2H-chromene
https://huagongshe.com/reaction/1679530
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 2-Chloro-N,N-dimethylethylamine | HCID 7901 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 4-(6-Methoxynaphthalen-2-yl)-2,2-dimethyl-2H-1-benzopyran-7-ol | HCID 20570493 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 2,2-dimethyl-7-(2-dimethylaminoethoxy)-4(6-methoxy-2-naphthyl)-2H-chromene | HCID 20570502 | — |
Reaktionsschritte
To a refluxing solution of 2,2-dimethyl-7-hydroxy-4(6-methoxy-2-naphthyl)-2H-chromene (6.4 g, 0.019 mole) and sodium hydride (1.4 g, 80% dispersion in oil) in toluene (150 ml) was added dropwise 2-dimethylaminoethyl chloride (2.7 g, 0.025 mole). After refluxing for 3 hours the solution was cooled and water added. The organic layer was separated and removal of the solvent gave a residue which dissolved in ether and extracted with dilute hydrochloric acid (3×). The combined acid extracts were basified with 40% sodium hydroxide solution and extracted with ether (3×). The combined ether extracts were dried and removal of the solvent gave a quantitative yield of 2,2-dimethyl-7-(2-dimethylaminoethoxy)-4(6-methoxy-2-naphthyl)-2H-chromene which was converted to the hydrochloride salt m.p. 96°-98° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04080335 |
|---|
| Quelldatensatz | uspto-grants-1978_03 |
|---|
| ORD ID | ord-4f14308f5ad5453a86f8f2c440060b7f |
|---|
| Quellennotiz | uspto-grants-1978_03 |
|---|