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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Octyltriphenylphosphonium bromide | HCID 3084855 | — |
| 반응물 | (1R,2R,3R)-2-(benzyloxymethyl)-3-methoxy-4,4-dimethylcyclohexane-1-carbaldehyde | HCID 54235868 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexamethylphosphoramide | HCID 12679 | — |
| 용매 | Butyllithium | HCID 178418339 | — |
| 생성물 | benzyl [(1R,2R,6S)-2-methoxy-3,3-dimethyl-6-[(E)-1-nonenyl]cyclohexyl]methyl ether | HCID 86748974 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05719291 |
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| 출처 데이터셋 | uspto-grants-1998_02 |
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| ORD ID | ord-7a33678808ce4f179937c39c9ad658f4 |
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| 출처 메모 | uspto-grants-1998_02 |
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