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HRID 493460作成日:2026年10月27日
Trichloro-2-propen-1-ylsilane → (4R,5R)-2-allyl-2-chloro-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolane
https://huagongshe.com/reaction/493460
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Trichloro-2-propen-1-ylsilane | HCID 7867 | — |
| 反応物 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 反応物 | (3R,4R)-2,5-dimethoxy-2,5-dimethyl-hexane-3,4-diol | HCID 11218000 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (4R,5R)-2-allyl-2-chloro-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolane | HCID 57681726 | 44.5% |
反応手順
Preparation of (4R,5R)-2-allyl-2-chloro-4,5-bis-(1-methoxy-1-methyl-[1,3,2]dioxasilolane: To a cooled (0° C.) solution of allyltrichlorosilane (7.0 mL; 48 mmol) in CH2Cl2 (80 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (15 mL; 102 mmol). A solution of (3R,4R)-2,5-dimethoxy-2,5-dimethyl-hexane-3,4-diol (10.0 g; 48 mmol) in CH2Cl2 (80 mL) was then added and the mixture was allowed to warm to ambient temperature and stirred for 12 hours. The solution was concentrated and the residue was treated with diethylether (100 mL). The mixture was stirred for 1 hour. The mixture was then filtered and the filtrate was concentrated. The residue was distilled under reduced pressure to give 6.6 g (44%) of (4R,5R)-2-allyl-2-chloro-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolane as a clear, colorless liquid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07534905B2 |
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| 出典データセット | uspto-grants-2009_05 |
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| ORD ID | ord-75b0dd9355294c39a606712ebada1dd7 |
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| 出典メモ | uspto-grants-2009_05 |
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