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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36066Erstellt: 24. Oktober 2026

Dimethylformamide → N-phenyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carboxamide

https://huagongshe.com/de/reaction/36066

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPhenyl isocyanateHCID 7672—
Edukt6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-oneHCID 14869554—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelAcetic AcidHCID 176—
ProduktN-phenyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carboxamideHCID 5471968021,4%

Reaktionsschritte

To a mixture of 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-one, 0.39 g of potassium t-butoxide, and 5 ml of dried N,N-dimethylformamide was added dropwise a mixture of 0.42 g of phenyl isocyanate and 1.5 ml of dried N,N-dimethylformamide while stirring under cooling with ice. After stirring for 4 hours under ice-cooling, ice-water was added thereto, and the mixture was made acidic with acetic acid and extracted with diethyl ether. The ether layer was washed with water and dried over sodium sulfate. Diethyl ether was removed by distillation, and the residue was purified by silica gel column chromatography (developing solution: CH2Cl2) to obtain 0.17 g of N-phenyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carboxamide represented by formula shown below.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05412117
Quelldatensatzuspto-grants-1995_05
ORD IDord-66ed7a06d95b4269b26ca4cfa7ade68e
Quellennotizuspto-grants-1995_05