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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2300412Erstellt: 26. Oktober 2026

Diketene → trans-4,4,4-Trifluoro-2-buten-1-yl acetoacetate

https://huagongshe.com/reaction/2300412

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiketeneHCID 12661—
Edukt4,4,4-Trifluoro-2-buten-1-olHCID 2777076—
KatalysatorSodium AcetateHCID 517045—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttrans-4,4,4-Trifluoro-2-buten-1-yl acetoacetateHCID 86758741154,6%

Reaktionsschritte

To a refluxing solution of 4,4,4-trifluoro-2-buten-1-ol (10 g, 79 mmol) and sodium acetate (0.51 g, 6.2 mmol) in anhydrous tetrahydrofuran (27 mL) under nitrogen, a solution of diketene (6.7 mL, 43.1 mmol) in anhydrous tetrahydrofuran (14 mL) was added dropwise over a period of 1 hour. The reaction mixture was heated at reflux for an additional 30 min upon completion of the addition. Then, the reaction mixture mixture was cooled to room temperature and diluted with diethyl ether (100 mL). The resulting solution was washed with a saturated aqueous sodium chloride solution (2×20 mL) and the organic layer was dried over sodium sulfate, filtered and the solvent removed under reduced pressure. The brown residue was purified by column chromatography using a mixture 4:1 of hexane and ethyl acetate as eluent to afford 14.0 g (84% yield) of trans-4,4,4-trifluoro-2-buten-1-yl acetoacetate as a colorless liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06498180B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-67b8eca8eae940b397db843fffd70999
Quellennotizuspto-grants-2002_12