HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 3-Benzyloxy-7-iodo-2-(3,4,5-trimethoxy-phenyl)chromen-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Hydroxy-7-iodo-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one | HCID 57887334 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Benzyloxy-7-iodo-2-(3,4,5-trimethoxy-phenyl)chromen-4-one | HCID 57887294 | 88% |
Reaction Steps
A stirring suspension of 3-hydroxy-7-iodo-2-(3,4,5-trimethoxyphenyl)-chromen-4-one (0.257 g, 0.6mmol), potassium carbonate (1.48 g, 11 mmol, 19 equ), potassium iodide (0.06 g, 0.3 mmol, 0.6 equ) and benzyl chloride (0.16 ml, 1.3 mmol, 2.3 equ) in acetone (12 ml) under nitrogen was heated to reflux for one hour. The reaction was filtered and the filtrate concentrated in vacuo to give an orange solid. This solid was recrystallised from isopropanol to give 34 (0.270 g, 88%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601754B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-d0a34b7ae8094572822d8f7dc9921116 |
| Source note | uspto-grants-2009_10 |