HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-(Allyloxy)-2-methoxy-1-(methylsulfanyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(Allyloxy)-2-sulfanylphenol | HCID 21877183 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(Allyloxy)-2-methoxy-1-(methylsulfanyl)benzene | HCID 21877148 | — |
Reaction Steps
5-(Allyloxy)-2-sulfanylphenol (37.84 g, 0.21 mol) and potassium carbonate (43 g, 0.31 mol) in acetone (450 ml) was cooled to 5° C. and treated with methyl iodide (32.32 ml, 0.52 mol) dropwise and stirred for 1 h at RT. After removal of the solvent in vacuo, the residue was partioned between diethyl ether (300 ml) and water (400 ml). The aqueous phase was separated and extracted with further diethyl ether (2×150 ml) and the combined organics were dried over MgSO4 and evaporated to a clear oil (26 g, 0.12 mol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07141586B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-4a589f2b4250443392094a9983cb5293 |
| Source note | uspto-grants-2006_11 |