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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 4-bromo-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran | HCID 10244628 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-azido-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran | HCID 10105169 | 97.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05393771 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-4fb4a803029948daa40f4c088aa414c8 |
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| Source note | uspto-grants-1995_02 |
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