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HRID 324003作成日:2026年10月25日

Ethyl isovalerate → (1-Ethoxy-3-methyl-but-1-enyloxy)-triisopropyl-silane

https://huagongshe.com/reaction/324003

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl isovalerateHCID 7945—
反応物TetrahydrofuranHCID 8028—
反応物Triisopropylsilyl trifluoromethanesulfonateHCID 2724529—
反応物Lithium HexamethyldisilazideHCID 2733832—
溶媒2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
生成物(1-Ethoxy-3-methyl-but-1-enyloxy)-triisopropyl-silaneHCID 53927273—

反応条件

温度-70 °C

反応手順

Tetrahydrofuran (100 ml) and 1,3-dimethyl-3,4,5,6-tetrahydro 2 (1H)-pyrimidinone (140 ml) were mixed at −20° C. and lithium bis (trimethylsilyl) amide (1M in tetrahydrofuran, 100 ml) was added. The mixture was cooled to −70° C., ethyl isovalerate (18.75 ml) added and stirred for ½ hour at −70° C. Triisopropylsilyl trifluoromethane sulfonate was added and the mixture left to stir at −75° C. for ½ hour before warming to room temperature and stirring for 3 hours. The reaction mixture was quenched with aqueous sodium bicarbonate (8%, 150 ml) and extracted with hexane (1000 ml). The hexane extract was washed with water (4×500 ml), dried (MgSO4), filtered and concentrated in vacuo to afford a crude yellow oil containing the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06215002B1
出典データセットuspto-grants-2001_04
ORD IDord-7bdf0bcac9b34bd9a369e584d6237570
出典メモuspto-grants-2001_04