HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → N-[4-bromo-3-(1-ethoxycarbonylbutyloxy)phenyl]-3,4,5,6-tetrahydrophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-bromovalerate | HCID 79071 | — |
| Reactant | N-(4-bromo-3-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 12769237 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[4-bromo-3-(1-ethoxycarbonylbutyloxy)phenyl]-3,4,5,6-tetrahydrophthalimide | HCID 15582848 | — |
Reaction Steps
A mixture of 15.0 g. of N-(4-bromo-3-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimide, 12.0 g. of ethyl α-bromovalerate, 7.7 g. of potassium carbonate, 2.5 g. of potassium iodide and 50 ml. of acetone was refluxed with stirring for 3 hours and then, the reaction mixture was cooled to room temperature and the salt was separated by a filtration. The filtrate was concentrated under a reduced pressure and 2N-HCl was added to the residue to crystallize the product. The crystal was separated by a filtration and washed with water and dried. The residue was purified by a chromatography on a column of silica gel (developing solvent: ethyl acetate: n-hexane of 1:3) to obtain 17.6 g. of Compound No. 90 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-4de79521328748efa30b11fa01c2c1d5 |
| Source note | uspto-grants-1985_08 |