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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329038생성일: 2026년 10월 25일

Sodium Iodide → 2-Butanol, 3-((1-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)-4-piperidinyl)oxy)-

https://huagongshe.com/reaction/329038

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물TriethylamineHCID 8471—
반응물10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
반응물1,2-Dimethyl-2-(4-piperidyloxy)-ethanolHCID 21440907—
용매Methyl Ethyl KetoneHCID 6569—
생성물2-Butanol, 3-((1-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)-4-piperidinyl)oxy)-HCID 21809348%

반응 단계

22.5 g (0.15 mole) of sodium iodide were added to a solution of 51.5 g (0.15 mole) of 10-(3-chloropropyl)-2-trifluoromethyl-phenothiazine in 400 ml of methyl ethyl ketone followed by the addition of 15.2 g (0.15 mole) of triethylamine and then 26 g (0.15 mole) of 1,2-dimethyl-2-(4-piperidyloxy)-ethanol. The mixture was then refluxed for 20 hours and after cooling, the precipitate formed was removed by vacuum filtration. The filtrate was evaporated to dryness and the oil residue was chromatographed over 1 kg of neutral alumina. Elution with ethyl acetate gave 34.5 g (48% yield) of 2-trifluoromethyl-10-[3-(4-[1,2-dimethyl-2-hydroxyethoxy]-piperidino)-propyl]-phenothiazine in the form of a clear amber oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04018922
출처 데이터셋uspto-grants-1977_04
ORD IDord-e8008bdff8df4e0796e205ef0c9844a3
출처 메모uspto-grants-1977_04