HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Quinoline-3-carbonyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Quinoline-3-carboxylic acid | HCID 80971 | — |
| Product | Quinoline-3-carbonyl Chloride | HCID 11030631 | — |
Reaction Steps
A 300 ml eggplant-shaped flask was equipped with a Dimroth condenser, a calcium chloride tube and a dropping funnel, and in the flask, 0.6 mol of thionyl chloride was slowly dropped to 0.1 mol of 3-quinolylcarboxylic acid with stirring at room temperature. After completion of the dropping, the resulting mixture was stirred continuously for about 1 hour on an oil bath at an oil bath temperature of 65° C. Thereafter, the excess thionyl chloride was removed under a reduced pressure to obtain 3-quinolylcarboxylic acid chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04449516 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-174559f5148f4569b93cf67afeb710e1 |
| Source note | uspto-grants-1984_05 |