HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 21555704, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178439523 | HCID 178439523 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 21555704 | HCID 21555704 | — |
Reaction Steps
A well-stirred mixture of 5 parts of ethyl 3-n-propyl-4-hydroxyquinoline-2-carboxylate, 3 parts of anhydrous potassium carbonate and 3.3 parts of benzyl bromide in anhydrous acetone was boiled under reflux for 16 hours, filtered to remove inorganic salts, and evaporated to remove solvent. A solution of the residual oil in 75 parts of ether, after being washed with N.sodium hydroxide (2 portions each comprising 25 parts) and then water (4 portions each of 40 parts) was dried over magnesium sulphate and evaporated to yield 6.4 parts of crude ethyl 3-n-propyl-4-benzyloxyquinoline-2-carboxylate as a very pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03941793 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-7c9266ba846c4d41b6c6a7ccb101663a |
| Source note | uspto-grants-1976_03 |