Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isopropanol | HCID 3776 | — |
| Edukt | Cycloheptanone | HCID 10400 | — |
| Edukt | Propane, 2,2',2''-[methylidynetris(oxy)]tris- | HCID 78191 | — |
| Edukt | Sodium bisulfate monohydrate | HCID 23673662 | — |
| Produkt | 1-Isopropoxy-1-cyclopentene | HCID 21997069 | 60,1% |
Reaktionsschritte
To a mixture of 56.0 grams (0.50 mol) of cycloheptanone, 107.0 grams (0.56 mol) of triisopropyl orthoformate and 44 grams of isopropanol (0.73 mol) in a 500 ml three-neck round bottom flask was added 2.8 grams (0.020 mol) of sodium hydrogensulfate monohydrate. Upon catalyst addition, the reaction temperature rose to 45° C., and was heated and maintained at 50° C. for about 5 hours. The progress of the reaction was monitored by GC until the ketone concentration was below 2%. The isopropanol and isopropyl formate by-products were removed by distillation under reduced pressure while the temperature of the reaction mixture was increased to a maximum of 60° C. The reaction mixture was cooled to room temperature and the pH value adjusted to about 7˜8 by adding 0.4 of gram potassium iso-propoxide. The mixture was then heated under reduced pressure to remove unreacted cycloheptanone and 1-isopropoxy-1-cyclopentene was isolated as a clear liquid at a yield of 60.1%. The purity of the product exceeded 98%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06235944B1 |
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| Quelldatensatz | uspto-grants-2001_05 |
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| ORD ID | ord-856b56f1e8e84a669727cbb1d07ea4d7 |
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| Quellennotiz | uspto-grants-2001_05 |
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