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 whole is heated under reflux. A solution of 19.4 g of 3-nitrophenol is then added dropwise thereto in the course of 2 hours and the whole is heated for a further 15 hours under reflux. The reaction mixture is filtered while hot and concentrated by evaporation. After chromatography of the residue over silica gel using toluene, 3-(3-bromopropoxy)-nitrobenzene is obtained in the form of a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863942 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-86790444b3984350a7417d8f286d44c9 |
| Source note | uspto-grants-1989_09 |