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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270983Erstellt: 25. Oktober 2026

Acetone → 1,6,6-Trimethyl-3-tert-butyl-fulvene

https://huagongshe.com/reaction/270983

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktDiethyl EtherHCID 3283—
EduktPyrrolidineHCID 31268—
Edukt1-Tert-butyl-3-methylcyclopenta-1,3-dieneHCID 15319844—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt1,6,6-Trimethyl-3-tert-butyl-fulveneHCID 2762761—

Reaktionsschritte

To a solution of 13.0 g (95.6 mmol) of 1-tert-butyl-3-methylcyclopentadiene in 130 ml of dehydrated methanol, 55.2 g (950.4 mmol) of dehydrated acetone was dropwise added in a nitrogen atmosphere at 0° C. with ice cooling, and 68.0 g (956.1 mmol) of pyrrolidine was further dropwise added, followed by stirring at room temperature for 4 days. After the reaction solution was diluted with 400 ml of diethyl ether, 400 ml of water was added. The organic phase was separated, washed with a 0.5N hydrochloric acid aqueous solution (150 ml×4), water (200 ml×3) and a saturated saline solution (150 ml), and then dried over anhydrous magnesium sulfate. The drying agent was filtered, and from the filtrate the solvent was distilled off to obtain a liquid. The liquid was subjected to vacuum distillation (70-80° C./0.1 mmHg) to obtain 10.5 g of a yellow liquid. The analyzed values are given below.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07449533B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-db3bd2deca0d4e5aab3042aaaca14277
Quellennotizuspto-grants-2008_11