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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275424Generated: October 25, 2026

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

https://huagongshe.com/reaction/275424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant4-bromo-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyranHCID 10244628—
SolventDimethylformamideHCID 6228—
Product4-azido-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyranHCID 1010516997.4%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05393771
Source datasetuspto-grants-1995_02
ORD IDord-4fb4a803029948daa40f4c088aa414c8
Source noteuspto-grants-1995_02