HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetylene → 1-Chloro-6-phthalimidohex-1-en-3-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetylene | HCID 6326 | — |
| Edukt | 4-(1,3-Dioxoisoindolin-2-yl)butanoyl chloride | HCID 594886 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Lösungsmittel | 1,1,2,2-Tetrachloroethane | HCID 6591 | — |
| Produkt | 1-Chloro-6-phthalimidohex-1-en-3-one | HCID 53737306 | — |
Reaktionsschritte
Aluminum chloride (43 g) is added to a stirred solution of 4-phthalimidobutyryl chloride (36.2 g) in 1,1,2,2-tetrachloroethane (400 ml), previously saturated with acetylene. Acetylene is bubbled through the solution overnight, with stirring, and the reaction mixture is then decomposed by the addition of crushed ice (300 g). The organic layer is separated and the aqueous layer extracted with 1,1,2,2-tetrachloroethane (3 × 100 ml). The combined organic solution is dried over sodium sulphate and concentrated. The residual solid is recrystallized from hexane affording 1-chloro-6-phthalimidohex-1-en-3-one, m.p. 92°C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US03968216 |
| Quelldatensatz | uspto-grants-1976_07 |
| ORD ID | ord-4080ad020c2844d3aae0d54dfe32d5fc |
| Quellennotiz | uspto-grants-1976_07 |