HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 1,2-Dihydro-6,7-dimethyl-2-oxo-3-quinolinecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 2-Chloro-6,7-dimethylquinoline-3-carbaldehyde | HCID 788657 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,2-Dihydro-6,7-dimethyl-2-oxo-3-quinolinecarbonitrile | HCID 13371428 | — |
Reaction Steps
A mixture was prepared from 15 g of 2-chloro-6,7-dimethyl-3-quinolinecarboxaldehyde, 5.4 g of hydroxylamine hydrochloride, 8.5 g of sodium formate and 155 ml of 97% formic acid and this was heated at reflux for 3 hours. Initially, the mixture became a heavy yellow paste but a homogeneous brown solution formed later. However, by the end of the 3-hour reflux period, the mixture was again heterogeneous and it was cooled and poured into 300 ml of water. The solid which formed was separated by filtration and dried to give 3-cyano-6,7-dimethyl-2(1H)-quinolinone melting at about 300° C. The indicated product contained 1/4 molecule of water of hydration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04735948 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-9cad88c2fabf4231a3512ca7624f7089 |
| Source note | uspto-grants-1988_04 |