HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220759Generated: October 30, 2026
Dimethylformamide → HCID 67425306, compound
https://huagongshe.com/reaction/220759
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 67425485 | HCID 67425485 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67425306 | HCID 67425306 | 33% |
Reaction Steps
7-{(diisopropylphosphoryl)-methyloxy}-3′,4′,5-trimethoxyflavone (0.5 g, 0.99 mmol, produced in Step 1 of Example 6) and sodium azide (0.5 g, 7.69 mmol) were added dropwise to N,N-dimethylformamide (20 mL) and warmed at 100° C. for 8 hours. The reaction solution was cooled to room temperature, and 50 mL of ethyl acetate and 50 mL of water were added dropwise, followed by separation of the organic layer from the aqueous layer. 10 mL of conc. hydrochloric acid was added dropwise to the aqueous layer which was then extracted with chloroform. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate and then evaporated to afford 0.15 g (yield: 33%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08203011B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-8568ad180a354dee97e28224b35d4954 |
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| Source note | uspto-grants-2012_06 |
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