HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1795113Erstellt: 24. Oktober 2026
1-Chloromethylnaphthalene → 2-(Naphthalen-1-ylmethoxy)benzaldehyde
https://huagongshe.com/de/reaction/1795113
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Chloromethylnaphthalene | HCID 6845 | — |
| Edukt | Salicylaldehyde | HCID 6998 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-(Naphthalen-1-ylmethoxy)benzaldehyde | HCID 885496 | 43,2% |
Reaktionsschritte
To a solution of 2-hydroxybenzaldehyde (2.30 g, 18.8 mmol) in DMF (20 mL) is added 1-(chloromethyl)-naphthalene (3.36 mL, 22.6 mmol) and K2CO3 (3.11 g, 22.6 mmol), and the reaction mixture is heated to 100° C. for 12 h. Once complete, the reaction mixture is cooled to room temperature and diluted with water (100 mL) prior to being poured into a separatory funnel containing ethyl acetate (250 mL). The organic layer is separated, washed with brine (2×) and dried over sodium sulfate prior to concentration. The crude product is purified by column chromatography (5% ethyl acetate in hexanes) to afford 2-(1-naphthylmethoxy)benzaldehyde (2.13 g, 43%) as a light yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07026339B2 |
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| Quelldatensatz | uspto-grants-2006_04 |
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| ORD ID | ord-3f39b2fc764a4dc582d690e962a26da4 |
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| Quellennotiz | uspto-grants-2006_04 |
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