HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20375617, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 20375643 | HCID 20375643 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20375617 | HCID 20375617 | 71% |
Reaction Steps
A solution of 4-(2-benzyloxyethyl)-6-fluoro-1-(3,4,5-tribromobenzyl)-1,2-dihydro-2-oxoquinoline (6.0 g.) in a mixture of dioxan (50 ml.), ethanol (50 ml.), and concentrated hydrochloric acid (2 ml.) was hydrogenated at atmospheric pressure over 5% palladium on carbon (1 g.). The theoretical quantity of hydrogen (390 ml. at N.T.P.) was absorbed in four minutes. The hydrogenation was stopped and the mixture filtered. Evaporation of the filtrate gave the crude product which was recrystallised twice from methanol to give 4-(2-hydroxyethyl)-6-fluoro-1-(3,4,5-tribromobenzyl)-1,2-dihydro-2-oxoquinoline, m.p. 199°-201° C., in 71% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04187310 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-e5f318db9e7a466db26eaf2ce364f3d7 |
| Source note | uspto-grants-1980_02 |