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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910769Generated: October 26, 2026

Water → Ethyl 1-[3-bromoprop-2-en-1-yl]-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate

https://huagongshe.com/reaction/910769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-DibromopropeneHCID 5201028—
ReactantEthyl 4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylateHCID 12876362—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-[3-bromoprop-2-en-1-yl]-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylateHCID 72343106—

Reaction Steps

Ethyl-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate (714 mg, 3.04 mmol) was suspended in degassed N,N-dimethylformamide (8 mL) and treated with 1,3-dibromo-1-propene (0.364 mL, 3.64 mmol, 1.2 equiv) and potassium carbonate (503 mg, 3.64 mmol, 1.2 equiv). After stirring for 7 hrs at ambient temperature, the mixture was poured into water and extracted three times with ethyl acetate. The combined ethyl acetate extracts were washed once with water and brine, dried with sodium sulfate, filtered and concentrated in vacuo to afforded ethyl 1-[3-bromoprop-2-en-1-yl]-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate as a mixture of E- and Z-isomers. Additional compound was obtained by concentration of the aqueous extract in vacuo and extraction of the resulting residue with a mixture of 80% chloroform and 20% methanol (v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022215B2
Source datasetuspto-grants-2011_09
ORD IDord-55a7999a8f44485ba64ad45c3368732a
Source noteuspto-grants-2011_09