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HRID 970030作成日:2026年10月26日

9-Borabicyclo(3.3.1)nonane → Ethyl(2S)-2-ethoxy-3-[4-(2-hydroxyethyl)phenyl]propanoate

https://huagongshe.com/reaction/970030

反応式

関与物質

役割名称HCID仕込み量
反応物9-Borabicyclo(3.3.1)nonaneHCID 78966—
反応物Trimethylamine oxide dihydrateHCID 198430—
反応物Ethyl(2S)-2-ethoxy-3-(4-vinylphenyl)propanoateHCID 69418759—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl(2S)-2-ethoxy-3-[4-(2-hydroxyethyl)phenyl]propanoateHCID 6941820562%

反応手順

9-BBN (3.0 mmol, 6 mL of a 0.5 M solution in hexanes) was added to a stirred solution of ethyl(2S)-2-ethoxy-3-(4-vinylphenyl)propanoate (0.37 g, 1.48 mmol) in dry THF under argon. The reaction mixture was stirred for 22 h under argon. Trimethylamine N-oxide dihydrate (0.60 g, 5.4 mmol) was added and the mixture was heated to reflux overnight and diluted with ether (50 mL). The organic layer was washed with brine (×3), dried (MgSO4), filtered, and evaporated. The crude product was purified by flash chromatography (silica, heptane/ethyl acetate 3:1) to give the title compound as an colorless oil (0.24 g, 62%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07309720B2
出典データセットuspto-grants-2007_12
ORD IDord-fbaf27d4bbad489bafbcd01e5ca17b24
出典メモuspto-grants-2007_12