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HRID 2399570作成日:2026年10月27日

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

https://huagongshe.com/reaction/2399570

反応式

関与物質

役割名称HCID仕込み量
反応物Octyltriphenylphosphonium bromideHCID 3084855—
反応物(1R,2R,3R)-2-(benzyloxymethyl)-3-methoxy-4,4-dimethylcyclohexane-1-carbaldehydeHCID 54235868—
溶媒TetrahydrofuranHCID 8028—
溶媒HexamethylphosphoramideHCID 12679—
溶媒ButyllithiumHCID 178418339—
生成物benzyl [(1R,2R,6S)-2-methoxy-3,3-dimethyl-6-[(E)-1-nonenyl]cyclohexyl]methyl etherHCID 8674897461%

反応条件

温度0 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05449785
出典データセットuspto-grants-1995_09
ORD IDord-cd09cab338264b0aa38c26ea9478047d
出典メモuspto-grants-1995_09