HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → N-[4-bromo-3-cyanomethoxyphenyl]-3,4,5,6-tetrahydrophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(4-bromo-3-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 12769237 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[4-bromo-3-cyanomethoxyphenyl]-3,4,5,6-tetrahydrophthalimide | HCID 13503460 | — |
Reaction Steps
A mixture of 1.0 g. of chloroacetonitrile, 2.2 g. of potassium iodide and 25 ml. of acetone was stirred at room temperature for 1 hour and then, 3.5 g. of N-(4-bromo-3-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimide and 1.8 g. of potassium carbonate were added and the mixture was refluxed with stirring for 5 hours. The solvent was distilled off under a reduced pressure and 2N-HCl was added to the residue to precipitate the product. The precipitate was separated by a filtration and washed with water and dried and recrystallized from ethanol to obtain 2.7 g. of Compound No. 229 shown in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536209 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-e31bd16767dc4611890a6257ed12acfc |
| Source note | uspto-grants-1985_08 |