HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropyl iodide → N-(2-Fluoro-5-isopropoxyphenyl)-3,4,5,6-tetrahydrophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(2-fluoro-5-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 13519181 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(2-Fluoro-5-isopropoxyphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 13556385 | 77.5% |
Reaction Steps
N-(2-Fluoro-5-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimide (VI) (10 g), isopropyl iodide (7 g) and anhydrous potassium carbonate (5.2 g) were dissolved in acetonitrile (100 ml), and the resultant solution was heated under reflux for 2.5 hours. After cooling, the reaction mixture was extracted with ethyl acetate. The extract was concentrated, and the precipitated crystals were collected by filtration to give 9 g of N-(2-fluoro-5-isopropoxyphenyl)-3,4,5,6-tetrahydrophthalimide (II: R=isopropyl). M.P. 62.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04563535 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-e0cc733b4d1e4119ac076070b0f760a5 |
| Source note | uspto-grants-1986_01 |