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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451474Generated: November 1, 2026

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

https://huagongshe.com/reaction/1451474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant6-Methoxy-9-fluorobenzo[g]isoquinoline-5,10-dioneHCID 10491359—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product9-Fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dioneHCID 10514352102.8%

Reaction Steps

A mixture of 9-fluoro-6-methoxybenzo[g]isoquinoline-5,10-dione (0.072 g) and aluminum trichloride (0.112 g) in dry methylene chloride (40 mL) is stirred at room temperature for 4 hours under a nitrogen atmosphere. An additional portion of aluminum chloride (0.190 g) is added and the mixture is allowed to react at reflux for 1.5 hrs and at room temperature overnight. Following addition of brine (15 mL) the aqueous phase is separated and extracted with methylene chloride (3×5 mL). The combined organic solutions are dried over anhydrous sodium sulphate and the solveht is removed by distillation at reduced pressure to give an approximately 1:1 mixture (0.070 g) of 9-fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dione (slower moving yellow spot on silica gel TLC plate, eluant methylene chloride/ethyl acetate 70/30) and 9-chloro-6-hydroxybenzo [g]isoquinoline-5,10-dione (faster moving yellow spot on the above chromatographic system) which is used without further purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604246
Source datasetuspto-grants-1997_02
ORD IDord-42c1badebfd541e1ab8b55dbc791c7a0
Source noteuspto-grants-1997_02