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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550816생성일: 2026년 10월 26일

Pyridine → 4-Hydroxy4-[3-(trifluoromethyl)phenyl]piperidine-1-carbonyl chloride

https://huagongshe.com/reaction/550816

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-[3-(Trifluoromethyl)phenyl]-4-piperidinolHCID 75255—
반응물TriphosgeneHCID 94429—
용매TetrahydrofuranHCID 8028—
생성물4-Hydroxy4-[3-(trifluoromethyl)phenyl]piperidine-1-carbonyl chlorideHCID 59011934203.6%

반응 단계

A solution of triphosgene (3.26 g, 0.011 mol) and anhydrous tetrahydrofuran (1000 mL) cooled to −20° C. was treated with pyridine (4.45 mL, 0.055 mol). The resulting cloudy suspension was slowly treated with a solution of 4-(3-trifluoromethyl-phenyl)-piperidin-4-ol (9 g, 0.036 mol) in anhydrous tetrahydrofuran (45 mL) while the internal temperature was maintained between −20° C. to −30° C. The resulting mixture was transferred to an ice bath which was allowed to come to 25° C. overnight to give a light brown solution with a small amount of brown precipitates. The reaction mixture was then concentrated in vacuo to give a brown solid. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 75/25 hexanes/ethyl acetate) afforded 4-hydroxy-4-(3-trifluoromethyl-phenyl)-piperidine-1-carbonyl chloride (6.89 g, 61%) as a clear, viscous oil. The NMR spectrum obtained on the sample is compatible with its structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947692B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-124a997a12b24ae5aab50a5ad76a1a59
출처 메모uspto-grants-2011_05