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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1643생성일: 2026년 10월 24일

Hydrochloric Acid → 6-[3-Adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoyloxy]-nicotinic acid

https://huagongshe.com/ko/reaction/1643

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TributylstannaneHCID 5948—
반응물Allyl 6-[3-adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoyl-oxy]-nicotinateHCID 21846704—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매TetrahydrofuranHCID 8028—
생성물6-[3-Adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoyloxy]-nicotinic acidHCID 2184671322.7%

반응 단계

100 mg of this ester were dissolved in 5 ml of absolute tetrahydrofuran and treated under argon with 104 mg of tetrakis-(triphenylphosphine)-palladium and 61 mg of tributyltin hydride. After stirring at room temperature for 30 min., the reaction mixture was poured on to ice/saturated ammonium chloride solution, acidified with 1N hydrochloric acid and extracted with ethyl acetate. The dark oil obtained after drying and evaporation was purified by chromatography (RP18-LiChroprep, acetonitrile) and recrystallization from ethyl acetate. There were obtained 21 mg of 6-[3-adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoyloxy]-nicotinic acid in colorless crystals, m.p. 188°-190° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726191
출처 데이터셋uspto-grants-1998_03
ORD IDord-429d4cda5f5a43799ceb5fbb3c399100
출처 메모uspto-grants-1998_03