HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → HCID 13470374, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 70577605 | HCID 70577605 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13470374 | HCID 13470374 | — |
Reaction Steps
A mixture of 3-methylsulphinyl-4-quinolone (1.035 g.), anhydrous potassium carbonate (1.38 g.), n-butyl bromide (0.685 g.) and dry acetone (50 ml.) was refluxed for 24 hours. The mixture was filtered and the filtrate evaporated to dryness. The resulting oil was dissolved in chloroform (50 ml.). The solution was washed with water, dried and evaporated. The residue oil was triturated with light petroleum to give the solid product 1-n-butyl-3-methylsulphinyl-4-quinolone, m.p. 103°-105°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04302460 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-5169342961b547a3bb30105cc0887b1a |
| Source note | uspto-grants-1981_11 |