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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1978249Erstellt: 25. Oktober 2026

Isopropanol → 1-Isopropoxy-1-cyclopentene

https://huagongshe.com/reaction/1978249

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
EduktCycloheptanoneHCID 10400—
EduktPropane, 2,2',2''-[methylidynetris(oxy)]tris-HCID 78191—
EduktSodium bisulfate monohydrateHCID 23673662—
Produkt1-Isopropoxy-1-cyclopenteneHCID 2199706960,1%

Reaktionsbedingungen

Temperatur50 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06235944B1
Quelldatensatzuspto-grants-2001_05
ORD IDord-856b56f1e8e84a669727cbb1d07ea4d7
Quellennotizuspto-grants-2001_05