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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 863176생성일: 2026년 10월 25일

Octyltriphenylphosphonium bromide → benzyl [(1R,2R,6S)-2-methoxy-3,3-dimethyl-6-[(E)-1-nonenyl]cyclohexyl]methyl ether

https://huagongshe.com/reaction/863176

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참여 물질

역할이름HCID투입량
반응물Octyltriphenylphosphonium bromideHCID 3084855—
반응물(1R,2R,3R)-2-(benzyloxymethyl)-3-methoxy-4,4-dimethylcyclohexane-1-carbaldehydeHCID 54235868—
용매TetrahydrofuranHCID 8028—
용매HexamethylphosphoramideHCID 12679—
용매ButyllithiumHCID 178418339—
생성물benzyl [(1R,2R,6S)-2-methoxy-3,3-dimethyl-6-[(E)-1-nonenyl]cyclohexyl]methyl etherHCID 8674897461%

반응 조건

온도0 °C

반응 단계

To a stirred solution of n-octyltriphenylphosphonium bromide (313 mg) in dry tetrahydrofuran (0.5 ml) and dry HMPA (0.5 ml), n-BuLi (0.44 ml, 1.6M solution in n-hexane) was added at 0° C. After the mixture was stirred at 0° C. for 30 min, a solution of (1R,2R,3R)-2-(benzyloxymethyl)-3-methoxy-4,4-dimethylcyclohexane-1-carbaldehyde (68 mg) in dry tetrahydrofuran (0.5 ml) was added to the resulting orange solution. The mixture was stirred at 0° C. for 30 min, and at room temperature for 2 hrs. The reaction was quenched by addition of saturated aqueous ammonium chloride solution. The mixture was extracted with diethyl ether, and the combined organic extracts were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was chromatographed on silica gel (using n-hexane:ethyl acetate=10:1 as an eluent) to give benzyl [(1R,2R,6S)-2-methoxy-3,3-dimethyl-6-[(E)-1-nonenyl]cyclohexyl]methyl ether (54 mg 61%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05719291
출처 데이터셋uspto-grants-1998_02
ORD IDord-7a33678808ce4f179937c39c9ad658f4
출처 메모uspto-grants-1998_02