HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287622Generated: October 29, 2026
Diethyl (ethoxymethylene)malonate → HCID 21408193, compound
https://huagongshe.com/reaction/1287622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | 6-Fluoro-2-methyl-2,3-dihydroquinolin-4(1H)-one | HCID 21408189 | — |
| Product | HCID 21408193 | HCID 21408193 | — |
Reaction Steps
A stirred mixture of 12 g (0.067 mole) of 6-fluoro-2-methyl-4-oxo-1,2,3,4-tetrahydroquinoline from example 4 and 14.8 g (0.070 mole) of diethyl ethoxymethylenemalonate was heated gradually to 160° to 180° C. while removing the ethanol generated by distillation. After 0.5 hour the mixture was cooled to 60° C., and 30 g of polyphosphoric acid was added. This mixture was heated gradually to 150 to 160° C. and maintained at 155° to 160° C. for 5 to 10 minutes. Following cooling, water was added, and the mixture was kneaded to produce an orange powder which was separated by filtration. Recrystallization from a mixture of 500 ml of 95% ethanol and 100 ml of glacial acetic acid gave a yellow product, ethyl 6,7-dihydro-1,7-dioxo-9-fluoro-5-methyl-1H,5H-benzo[ij]-quinolizine-2-carboxylate, m.p. 262°-265° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03985753 |
|---|
| Source dataset | uspto-grants-1976_10 |
|---|
| ORD ID | ord-20d0d648ae4f4173b02884af5c684492 |
|---|
| Source note | uspto-grants-1976_10 |
|---|