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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245058Generated: November 1, 2026

Ethanol → Ethyl 7-bromoisoquinoline-3-carboxylate

https://huagongshe.com/reaction/1245058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium ethoxideHCID 2723922—
Reactant4-Bromobenzene-1,2-dicarbaldehydeHCID 13255257—
ReactantHCID 86592791HCID 86592791—
ProductEthyl 7-bromoisoquinoline-3-carboxylateHCID 6908343478%

Reaction Steps

A mixture of 4-bromo-benzene-1,2-dicarbaldehyde (0.450 g, 2.137 mmol), diethylamino malonate (0.452 g, 2.137 mmol), and sodium ethoxide (0.218 g, 3.20 mmol) in anhydrous ethanol (15 mL) was refluxed for 4 hr. The solution was cooled to rt and concentrated under reduced pressure. The crude residue was purified by flash column chromatography (silica gel, 0.5% MeOH in CHCl3) to obtain 0.460 g (78%) of the 7-bromo-isoquinoline-3-carboxylic acid ethyl ester which was hydrolyzed according to general procedure C yielding the 0.350 g (85%) of 7-bromo-isoquinoline-3-carboxylic acid as a white solid. LC/MS (m/z): 253 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122580B2
Source datasetuspto-grants-2006_10
ORD IDord-38b03af3006b4d4ab672cf9980649715
Source noteuspto-grants-2006_10