化工社化工社 化学情報印刷レポート · 研究参考用
9-Borabicyclo(3.3.1)nonane → Ethyl(2S)-2-ethoxy-3-[4-(2-hydroxyethyl)phenyl]propanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| 反応物 | Trimethylamine oxide dihydrate | HCID 198430 | — |
| 反応物 | Ethyl(2S)-2-ethoxy-3-(4-vinylphenyl)propanoate | HCID 69418759 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Ethyl(2S)-2-ethoxy-3-[4-(2-hydroxyethyl)phenyl]propanoate | HCID 69418205 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07309720B2 |
| 出典データセット | uspto-grants-2007_12 |
| ORD ID | ord-fbaf27d4bbad489bafbcd01e5ca17b24 |
| 出典メモ | uspto-grants-2007_12 |