HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1030850Erstellt: 26. Oktober 2026
Hydrochloric Acid → 2-(6-Methoxynaphthalen-2-yl)propanenitrile
https://huagongshe.com/reaction/1030850
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Edukt | 2-(5-Bromo-6-methoxy-2-naphthyl)propionitrile | HCID 14073055 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Mesitylene | HCID 7947 | — |
| Produkt | 2-(6-Methoxynaphthalen-2-yl)propanenitrile | HCID 607344 | 71% |
Reaktionsschritte
10 Grams of anhydrous aluminum chloride are added portionwise and under stirring to a solution containing 14.5 g of 2-(5-bromo-6-methoxy-2-naphthyl)propionitrile dissolved in 60 ml of methylene chloride and 8.3 ml of mesitylene, while keeping the temperature at about 20° C. The reaction mixture is kept at this temperature under stirring for 1 hour and then is slowly poured into a mixture made of 60 g of crushed ice and of 20 ml of a 6N aqueous solution of hydrochloric acid. The layers are separated after 15 minutes of stirring and the aqueous layer is discarded. The organic layer is twice washed with 25 ml of a 6N aqueous solution of hydrochloric acid, then with 25 ml of water and is dried over anhydrous sodium sulfate. The organic solution is evaporated to dryness under vacuum and the residue is crystallized from tetrachloroethylene obtaining 7.5 g of product with a yield of 71%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05107013 |
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| Quelldatensatz | uspto-grants-1992_04 |
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| ORD ID | ord-ae40c9524c794c9f9020bfc134b647e7 |
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| Quellennotiz | uspto-grants-1992_04 |
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