HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327528Generated: October 27, 2026
Potassium Iodide → HCID 10429859, compound
https://huagongshe.com/reaction/327528
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(4-Bromobutyl)phthalimide | HCID 93575 | — |
| Reactant | 5-Methoxy-3,4-dihydro-2H-1-benzopyran-3-amine | HCID 13928948 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10429859 | HCID 10429859 | 67% |
Reaction Steps
In a round bottomed flask, 2.2 mmol of 3-amino-5-methoxychroman (described in Patent EP 279,150) are dissolved in 6 ml of dimethylformamide in the presence of 2.4 mmol of N-(4-bromobutyl)phthalimide, 6.6 mmol of potassium carbonate and a catalytic amount of potassium iodide. The mixture is left stirring at 60° C. for 6 hours. After cooling, the solvent is evaporated off and, after aqueous hydrolysis, the crude reaction mixture is extracted with dichloromethane. After washing, drying and evaporation of the organic phase, the expected product is obtained after purification by chromatography on a silica column (elution solvent: ether/petroleum ether, 5:95).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05273994 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-befe2eb590994bd7a83c968217259e12 |
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| Source note | uspto-grants-1993_12 |
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