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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275424Erstellt: 27. Oktober 2026

Sodium Azide → 4-azido-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran

https://huagongshe.com/reaction/275424

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium AzideHCID 33557—
Edukt4-bromo-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyranHCID 10244628—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-azido-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyranHCID 1010516997,4%

Reaktionsschritte

A solution of 4-bromo-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran (6.73 g, 25.29 mmoles), title B compound, in dry N,N-dimethylformamide (100 mL) was treated with sodium azide (3.79 g, 50.57 mmoles) and stirred at room temperature under argon for 4 hours. The reaction mixture was partitioned between 100 mL ethyl acetate and 200 mL distilled water. The organic layer was separated and the aqueous layer was extracted with 100 mL of ethyl acetate. The combined organics were washed successively with distilled water, saturated sodium bicarbonate solution, brine and dried over magnesium sulfate. The solvent was evaporated under vacuum to obtain an orange gum (5.62 g) which was triturated with pentane to provide the title compound (4.50 g, 78%) as an off-white solid, m.p. 63°-64° C. Microanalysis calculated for C12H12N4O: C, 63.15; H, 5.30; N, 24.55. Found: C, 63.57; H, 5.27; N, 24.75.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05393771
Quelldatensatzuspto-grants-1995_02
ORD IDord-4fb4a803029948daa40f4c088aa414c8
Quellennotizuspto-grants-1995_02