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HRID 579505作成日:2026年10月26日
HCID 66832833、化合物 → 3-Benzyl 4-ethyl 2,2-dimethyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butyl)oxazolidine-3,4-dicarboxylate
https://huagongshe.com/reaction/579505
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | HCID 66832833 | HCID 66832833 | — |
| 反応物 | HCID 178419189 | HCID 178419189 | — |
| 触媒 | 1,2-Bis(diphenylphosphino)ethane | HCID 74267 | — |
| 触媒 | Chloro(1,5-cyclooctadiene)iridium(I) dimer | HCID 6436381 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-Benzyl 4-ethyl 2,2-dimethyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butyl)oxazolidine-3,4-dicarboxylate | HCID 66833605 | 65.3% |
反応手順
While under an argon atmosphere, a solution of chloro(1,5-cyclooctadiene) iridium(I) dimer (15 mg, 0.022 mmol) and 1,2-bis(diphenyl-phosphino) ethane (18 mg, 0.044 mmol) in dichloromethane (5 mL) was treated with pinacol borane (225 mg, 1.76 mmol, 0.26 mL) and stirred for 15 minutes. To this mixture was added a solution of 3-benzyl 4-ethyl 4-(but-3-enyl)-2,2-dimethyloxazolidine-3,4-dicarboxylate (530 mg, 1.47 mmol) in dichloromethane (5 mL). After stirring for 19 h at room temperature the solution was concentrated and purified using a combiflash system (24 g column, eluting with 5-50% (ethyl acetate in heptanes) to give 3-benzyl 4-ethyl 2,2-dimethyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butyl)oxazolidine-3,4-dicarboxylate (470 mg, 65%). 1H NMR (CDCl3) δ: 7.22 (m, 5H), 5.01 (m, 2H), 3.91 (m, 4H), 2.20-2.01 (m, 1H), 1.75 (m, 1H), 1.51 (2s, 6H), 1.29 (m, 4H), 1.16 (s, 12H), 1.02 (t, J=7.2 Hz, 3H), 0.69 (t, 2H). MS found for C26H40BNO7 m/z [490 (M+1), 522 (M+Na)].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09040703B2 |
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| 出典データセット | uspto-grants-2015_05 |
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| ORD ID | ord-e47af45f283f4e74866134f98b723080 |
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| 出典メモ | uspto-grants-2015_05 |
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