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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1613935생성일: 2026년 10월 27일

Hexamethylphosphorous triamide → 2-(trans-1-Nonenyl)-3-methyl-4-acetoxy-6-fluoroquinoline

https://huagongshe.com/reaction/1613935

반응식

참여 물질

역할이름HCID투입량
반응물Hexamethylphosphorous triamideHCID 15355—
반응물Octyltriphenylphosphonium bromideHCID 3084855—
반응물2-Formyl-3-methyl-4-acetoxy-6-fluoroquinolineHCID 15007058—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물2-(trans-1-Nonenyl)-3-methyl-4-acetoxy-6-fluoroquinolineHCID 1500705910.2%

반응 단계

0.29 ml of a hexane solution of 0.48 mmols of n-butyl lithium was added to a solution of 218 mg (0.48 mmols) of octyltriphenylphosphonium bromide in 3 ml of tetrahydrofuran and stirred at room temperature for 5 minutes. This solution was cooled to -78° C., after which 1.43 g (8 mmols) of hexamethylphosphorus triamide was added and stirred for 5 minutes, followed by further addition of 2 ml of a tetrahydrofuran solution of 98.8 mg (0.40 mmols) of 2-formyl-3-methyl-4-acetoxy-6-fluoroquinoline and stirring at -78° C. for 15 minutes and -42° C. for 30 minutes. The reaction solution was added to 20 ml of water and extracted with ethyl acetate, followed by washing with a saturated sodium chloride aqueous solution and drying with anhydrous sodium sulfate. After removal of the solvent by distillation under reduced pressure, the residue was purified by silica gel column chromatography (solvent n-hexane ethyl acetate=30:1 ) to obtain 14 mg (yield 10 %) of 2-(trans-1-nonenyl)-3-methyl-4-acetoxy-6-fluoroquinoline.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05194617
출처 데이터셋uspto-grants-1993_03
ORD IDord-8c551084591e4f9f836d35e9bd028b88
출처 메모uspto-grants-1993_03