HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 54082516, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sesamol | HCID 68289 | — |
| Reactant | HCID 54298637 | HCID 54298637 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 54082516 | HCID 54082516 | — |
Reaction Steps
2.35 g (0.017 mol) of potassium carbonate and 50 mg of potassium iodide are added to a solution of 4.0 g (0.017 mol) of 1-bromo-6-isopropoxy-4-methyl-3-hexene and 2.35 g (0.017 mol) of 3,4-methylendioxy-phenol in 120 cc of acetone. The suspension is boiled under reflux during the course of 20 hours, is then filtered and liberated from acetone in a vacuum. The residue is taken up in ether, washed with water and saturated salt solution, dried over sodium sulphate and evaporated. The residue is chromatographed on silica gel with hexane/ethyl acetate 9:1. Thus the cis/trans isomeric mixture of the 5-(6-isopropoxy-4-methyl methyl-3-hexenyloxy)-1,3-benzodioxol is obtained as colourless oil. nD20 = 1.5111.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03968235 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-e1abc156563249ed8c72239fc4d2a43f |
| Source note | uspto-grants-1976_07 |