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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

反応式

関与物質

役割名称HCID仕込み量
反応物Trichloro-2-propen-1-ylsilaneHCID 7867—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物(3R,4R)-2,5-dimethoxy-2,5-dimethyl-hexane-3,4-diolHCID 11218000—
溶媒DichloromethaneHCID 6344—
生成物(4R,5R)-2-allyl-2-chloro-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolaneHCID 5768172644.5%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07534905B2
出典データセットuspto-grants-2009_05
ORD IDord-75b0dd9355294c39a606712ebada1dd7
出典メモuspto-grants-2009_05