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HRID 234808作成日:2026年10月25日

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

https://huagongshe.com/reaction/234808

反応式

関与物質

役割名称HCID仕込み量
反応物Aluminum(III) ChlorideHCID 6451240—
反応物6-Methoxy-9-fluorobenzo[g]isoquinoline-5,10-dioneHCID 10491359—
溶媒DichloromethaneHCID 6344—
溶媒Sodium chloride; waterHCID 57417360—
生成物9-Fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dioneHCID 10514352102.8%

反応手順

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 solvent 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05596097
出典データセットuspto-grants-1997_01
ORD IDord-38bc3982e19d4bd391f75be4d9973282
出典メモuspto-grants-1997_01