HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 2-((4-(Trifluoromethyl)phenoxy)methyl)oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Trifluoromethyl)phenol | HCID 67874 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-((4-(Trifluoromethyl)phenoxy)methyl)oxirane | HCID 22282752 | — |
Reaction Steps
5 g of 4-hydroxybenzotrifluoride, 12.8 g of potassium carbonate, 500 mg of potassium iodide and 18 g of epichlorohydrin are stirred in 75 ml of acetone for 15 hours at 60° C. The reaction mixture is filtered and the filtrate is concentrated. The residue is taken up in ethyl acetate and washed with water. After concentration of the organic phase and Kugelrohr distillation, 2-(4-trifluoromethyl-phenoxymethyl)-oxirane is obtained. (b.p.20 145-150° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07638514B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-8d9d29ad5727471faa3572dc34c7396e |
| Source note | uspto-grants-2009_12 |