HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418240Generated: November 2, 2026
Diethyl (ethoxymethylene)malonate → HCID 13577655, compound
https://huagongshe.com/reaction/2418240
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | HCID 13577654 | HCID 13577654 | — |
| Reactant | HCID 20248485 | HCID 20248485 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 13577655 | HCID 13577655 | — |
Reaction Steps
A mixture of 1.2 g of 6-fluoro-5-methoxy-1,2,3,4-tetrahydroquinaldine and 2.5 g of diethyl ethoxymethylenemalonate was heated at 140° C. for 3 hours, and was then cooled to 100° C. To the crude hot diethyl 2-[N-(6-fluoro-5-methoxy-1,2,3,4-tetrahydroquinaldinyl)]methylenemalonate was added 25 g of polyphosphoric acid, and the mixture was heated on a steam bath for one hour. The mixture containing ethyl 6,7-dihydro-9-fluoro-8-methoxy-5-methyl-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylate was cooled to about 20° C., diluted with an equal volume of water and basified with 50% sodium hydroxide solution. This solution was heated at its reflux temperature for two hours and filtered hot through celite. The filtrate was cooled to about 20° C. and acidified with concentrated hydrochloric acid. The solid was separated by filtration to provide 1.2 g of off-white 6,7-dihydro-9-fluoro-8-methoxy-5-methyl-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid. Recrystallization from aqueous N,N-dimethylformamide provided pure product, m.p. 234°-236° C. Analysis: Calculated for C15H14FNO4 : %C, 61.8; %H, 4.8; %N, 4.8; Found: %C, 61.7; %H, 4.6; %N, 4.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04472407 |
|---|
| Source dataset | uspto-grants-1984_09 |
|---|
| ORD ID | ord-da88de391790417eb5ea4c1e964fa122 |
|---|
| Source note | uspto-grants-1984_09 |
|---|