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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 569651생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/569651

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물Potassium HydroxideHCID 14797—
반응물6-Chloro-2-tetraloneHCID 4456139—
반응물1-Propanamine, 3-chloro-, hydrochlorideHCID 11469095—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매TriethylamineHCID 8471—
생성물4-Acetyl-8-chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinolineHCID 19833119—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04732979
출처 데이터셋uspto-grants-1988_03
ORD IDord-c7fc9ef211134df49f8793ce57eb19c2
출처 메모uspto-grants-1988_03