HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-chloro-N-(8-quinolyl)butyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 8-Aminoquinoline | HCID 11359 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-chloro-N-(8-quinolyl)butyramide | HCID 12898546 | 53% |
Reaction Steps
A solution of 8-aminoquinoline (10 L g, 0.069 mole) and triethylamine (10 ml, 0.072 mole) in dry tetrahydrofuran (40 ml) was treated dropwise at room temperature with 4-chlorobutyryl chloride (about 0.07 mole) until the green reaction mixture turned yellow in colour. The reaction was filtered and the solids (triethylamine hydrochloride) were washed with tetrahydrofuran. The combined filtrates were concentrated by vacuum distillation, (≃15 mm Hg), filtered over alumina in methylene chloride, concentrated and recyrstallized from ether/petroleum ether affording 4-chloro-N-(8-quinolyl)butyramide. An analytical sample was prepared by recrystallization (m.p. 62°-63°), yield 53%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04366158 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-ddf634dbbf72471799d7274361139b10 |
| Source note | uspto-grants-1982_12 |