HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-(3-Bromopropoxy)-3-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | 3-Nitrophenol | HCID 11137 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(3-Bromopropoxy)-3-nitrobenzene | HCID 7172301 | — |
Reaction Steps
43 ml of 1,3-dibromopropane are added to a suspension of 29 g of potassium carbonate and 0.5 g of potassium iodide in 170 ml of acetone and the mixture is refluxed. A solution of 19.4 g of 3-nitrophenol is then added dropwise in the course of 2 hours and the mixture is refluxed for a further 15 hours. The reaction mixture is filtered hot and evaporated. Chromatography of the residue on silica gel with toluene gives 3-(3-bromopropoxy)-nitrobenzene as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670604 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-7262511741cc431fb3813f52b11f02e2 |
| Source note | uspto-grants-1987_06 |