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HRID 569651作成日:2026年10月27日

Acetyl chloride → 4-Acetyl-8-chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline

https://huagongshe.com/reaction/569651

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物Potassium HydroxideHCID 14797—
反応物6-Chloro-2-tetraloneHCID 4456139—
反応物1-Propanamine, 3-chloro-, hydrochlorideHCID 11469095—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒TriethylamineHCID 8471—
生成物4-Acetyl-8-chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinolineHCID 19833119—

反応手順

100 g (0.55 mol) of 6-chloro-3,4-dihydro-2(1H)-naphthalenone were dissolved in 2 l of toluene under argon, treated with 64.0 g of powdered potassium hydroxide, heated to boiling temperature, 165 g of 3-chloropropylamine hydrochloride were added portionwise thereto during 30 minutes and the mixture was boiled on a water separator until educt can no longer be detected in a thin-layer chromatogram. After cooling to room temperature the mixture was treated with 155 ml of triethylamine. The mixture was treated dropwise with 60 ml of acetyl chloride dissolved in 450 ml of toluene while cooling with ice so that an internal temperature of 25° was not exceeded. The mixture was stirred at room temperature for 1 hour, extracted with water/methylene chloride, dried with magnesium sulphate, the solvent was distilled off in vacuo and there was obtained 4-acetyl-8-chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline in the form of brown crystals which can be employed as the crude product for the reaction described hereinafter.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04732979
出典データセットuspto-grants-1988_03
ORD IDord-c7fc9ef211134df49f8793ce57eb19c2
出典メモuspto-grants-1988_03