HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 12802695, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | {1-[(4-Nitrophenyl)methyl]-2-oxo-1,2-dihydroquinolin-4-yl}acetonitrile | HCID 12802694 | — |
| Product | HCID 12802695 | HCID 12802695 | — |
Reaction Steps
1-(4-Nitrobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetonitrile (0.5 g.) was added to a solution of sodium hydroxide (0.2 g.) in ethanol (50 ml.) and the mixture was heated under reflux for 5 hours. The ethanol was evaporated under reduced pressure and the residue was treated with 2 N hydrochloric acid (100 ml.). The precipitate thus formed was separated off and recrystallised from ethanol to give 1-(4-nitrobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid (0.42 g.) m.p. 208°-210° C., (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04187310 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-e730387c156a4bca84986b35046532a0 |
| Source note | uspto-grants-1980_02 |