HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → 2-(3-Ethoxyphenyl)-4,5-dihydropyrazolo[1,5-a]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Phenol, 3-(4,5-dihydropyrazolo(1,5-a)quinolin-2-yl)- | HCID 3042689 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(3-Ethoxyphenyl)-4,5-dihydropyrazolo[1,5-a]quinoline | HCID 13412513 | — |
Reaction Steps
2.62 Grams (0.010 mole) of the compound of Example 10 is added to a solution of 0.23 g. (0.010 mole) of sodium in 40 ml. of absolute ethanol at room temperature, then 2.2 g. (0.020 mole) of ethyl bromide is added dropwise. The resulting solution is refluxed for seven hours and allowed to stand overnight at room temperature. After dilution with 30 ml. of water and subsequent evaporation of the ethanol, a residue is obtained which is crystallized from methanol. Yield 2.29 g. of the title compound, m.p. 99°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024149 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-5ee4a91051b24501ab41c0447622520e |
| Source note | uspto-grants-1977_05 |