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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 6-Methoxy-9-fluorobenzo[g]isoquinoline-5,10-dione | HCID 10491359 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 9-Fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dione | HCID 10514352 | 102.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05604246 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-42c1badebfd541e1ab8b55dbc791c7a0 |
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| Source note | uspto-grants-1997_02 |
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