HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → HCID 66783913, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Kanzakiflavone 2 | HCID 44258472 | — |
| Reactant | HCID 44258636 | HCID 44258636 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66783913 | HCID 66783913 | — |
Reaction Steps
A solution of Kanzakiflavone-1 or 6,7-methylenedioxy-5,4′-dihydroxyflavone (1.49 g, 5 mmol) [Manchanda, V. P.; Khanna, R. N. Curr. Sci. (1977), 46(13), 445-6.] and dimethylsulfate (1.02 g, 8 mmol) in acetone (20 ml) is refluxed in the presence of anyhyd. potassium carbonate (0.5 g) overnight. The reaction mixture is filtered off and the filtrate is evaporated to give a dark brown residue. The residue is taken up in ethyl acetate and washed with water followed by saturated brine solution and dried (MgSO4), thus giving the title compound, upon filtration and evaporation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138165B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-45e0ea236fc94c6e9712977fa6370c90 |
| Source note | uspto-grants-2012_03 |