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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 727389Erstellt: 25. Oktober 2026

Acetic Anhydride → HCID 15871313, Verbindung

https://huagongshe.com/reaction/727389

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktTriethylamineHCID 8471—
Edukt1,1,1-TrimethoxybutaneHCID 123512—
Edukt[2,6-Dichloro-4-(trifluoromethyl)phenyl]hydrazineHCID 688223—
Edukt2,5-DimethylbenzoylacetonitrileHCID 15895264—
Edukt1-Cyano-1-(2,5-dimethylbenzoyl)-3-methoxy-1-penteneHCID 53648846—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 15871313HCID 15871313—

Reaktionsschritte

A solution of 0.52 g (3.0 mmol) of 2,5-dimethylbenzoylacetonitrile, 0.45 g (3.0 mmol) of trimethylorthobutyrate and 0.632 g (0.58 mL, 6.2 mmol) of acetic anhydride in 5.0 mL of ethyl acetate was refluxed overnight and then cooled. The solvents were removed in vacuo and the residues were dissolved in 10 mL of ethanol. One-half of this solution, containing 1.5 mmol of 1-cyano-1-(2,5-dimethylbenzoyl)-3-methoxy-1-pentene was mixed with 0.7 mL (0.51 g, 5.0 mmol) of triethylamine and 0.37 g (1.50 mmol) of 2,6-dichloro-4-trifluoromethylphenylhydrazine and refluxed for 2.5 hours. The reaction mixture was cooled and partitioned between dilute hydrogen chloride and ethyl acetate. The organic phase was washed with water and then dried with brine and with magnesium sulfate. The solvent was evaporated to give an oil which was chromatographed on silica gel by the flash method eluting with 4:1 hexane/ethyl acetate to give the title compound as an amorphous foam. Anal. Calcd. for C22H20ON3CL2F3, 469.0935. Found: 469.0889.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05712303
Quelldatensatzuspto-grants-1998_01
ORD IDord-fbc3da8862f144fd81839583d69cc429
Quellennotizuspto-grants-1998_01