HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 572698Erstellt: 25. Oktober 2026
Tetrahydrofuran → 2-(7-Methoxynaphthalen-1-yl)acetonitrile
https://huagongshe.com/reaction/572698
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Trifluoroacetic anhydride | HCID 9845 | — |
| Edukt | 2-(7-Methoxynaphthalen-1-yl)acetamide | HCID 15149127 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 2-(7-Methoxynaphthalen-1-yl)acetonitrile | HCID 11264068 | 101,9% |
Reaktionsschritte
30 g 7-methoxy-1-naphthaleneacetamide, 120 ml THF and 35.7 g triethylamine were added into reaction flask. The mixture was stirred and cooled with external ice saline bath. Trifluoroacetic anhydride was slowly added in drops. After completion of addition, it was stirred for further 15 min. Then, the ice bath was removed and stirring was carried out for 2 h at room temperature. After completion of the reaction, the reaction solution was evaporated. Subsequently, 200 ml water was added and the solution was filtered and dried after stirring for 0.5 hours, to obtain 28 g crude product. Recrystallization was carried out using 280 ml isopropyl ether and 1.4 g activated carbon to obtain 22 g refined product with the mp of 82-84° C. The yield is 80%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09029420B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-113758f9cfd74f74a0d617ade4459445 |
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| Quellennotiz | uspto-grants-2015_05 |
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