HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-Iodo-3-methoxy-5-(trifluoromethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 5-(Trifluoromethyl)-m-anisidine | HCID 605671 | — |
| Product | 1-Iodo-3-methoxy-5-(trifluoromethyl)benzene | HCID 19773106 | — |
Reaction Steps
Using conventional procedures 3-methoxy-5-trifluoromethylaniline (J. Chem. Soc., 1951, 2013) was diazotised and reacted with potassium iodide to give 3-methoxy-5-trifluoromethyliodobenzene, as an oil. The product so obtained was reacted with boro tribromide using the conditions described in Note b. above to give 3-hydroxy-5-trifluoromethyliodobenzene in 95% yield, as an oil. The product so obtained was reacted with 2-bromomethylnaphthalene using the conditions described in Example 1 to give 3-(naphth-2-ylmethoxy)-5-trifluoromethyliodobenzene in 62% yield, m.p. 65°-66° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05089513 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-eff0f9e0dd5141ffa7aabc13911b0a5d |
| Source note | uspto-grants-1992_02 |