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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451475Generated: October 27, 2026

Aluminum(III) Chloride → 9-Fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dione

https://huagongshe.com/reaction/1451475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant6-Methoxy-9-fluorobenzo[g]isoquinoline-5,10-dioneHCID 10491359—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product9-Fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dioneHCID 10514352—
Product9-Chloro-6-hydroxybenzo[g]isoquinoline-5,10-dioneHCID 10777706—

Reaction Steps

Aluminum chloride (19.05 g) is added in one portion to a stirred refluxing solution of 6-methoxy-9-fluorobenzo[g]isoquinoline-5,10-dione (7.20 g) in methylene chloride (432 mL). After refluxing for 4 hours the reaction mixture is cooled and poured in water (1,300 mL). Methylene chloride (200 mL) is added and after stirring for 10 min the organic phase is separated. The aqueous solution is saturated with NaCl and further extracted with methylene chloride (3×400 mL). The combined organic solutions are washed with brine (1,000 mL), dried and the solvent removed by roto-evaporation. The brown solid obtained (6.5 g) is recrystallized from ethyl acetate/n-hexane 1/1 (65 mL) to yield a 9/1 mixture (1H-NMR evaluation) of 9-fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dione and 9-chloro-6-hydroxybenzo[g]isoquinoline-5,10-dione respectively (6.00 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604246
Source datasetuspto-grants-1997_02
ORD IDord-b9fc49e5a0fb4235b7e3b189a1c6d519
Source noteuspto-grants-1997_02