HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10909Generated: October 29, 2026
Potassium Iodide → 2-Azido-N-(beta-oxo-2,5-dimethoxy phenehyl)acetamide
https://huagongshe.com/reaction/10909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 2-Chloro-N-(b-oxo-2,5-dimethoxy-phenylethyl)-acetamid | HCID 11637604 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Azido-N-(beta-oxo-2,5-dimethoxy phenehyl)acetamide | HCID 11572675 | 91% |
Reaction Steps
In a four neck round bottomed flask, 45 gm (0.165 mole) of 2-Chloro-N-(β-oxo-2,5-Dimethoxy phenethyl)-acetamide prepared according to step (b), 27 g (0.415 mole) sodium azide and 8.3 g (0.049 mole) potassium iodide and 900 ml of acetone is charged. The solution is refluxed at 60° C. for 5 hours. After completion of the reaction the reaction mass cooled and filtered to remove inorganics. Acetone is distilled off under atmospheric pressure. Water is added and the resulting yellow lumps are filtered. (Yield: 91%). The solid is recrystallized from methanol. The following physical properties are measured.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094928B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-8c23ebe7c2534221923202bb5e04eb41 |
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| Source note | uspto-grants-2006_08 |
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