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HRID 2283430作成日:2026年10月27日

Chlorotrimethylsilane → (1-Isobutoxy-2-methyl-propenyloxy)-trimethyl-silane

https://huagongshe.com/reaction/2283430

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物Isobutyl isobutyrateHCID 7351—
反応物DiisopropylamineHCID 7912—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物(1-Isobutoxy-2-methyl-propenyloxy)-trimethyl-silaneHCID 1562627677.8%

反応条件

温度0 °C

反応手順

Step 1 To a solution of diisopropylamine (2.94 mL, 20.8 mmol) in THF (20 mL) under nitrogen at 0° C. was added nBuLi (2.5M in hexanes, 8.32 mL, 20.8 mmol, 1 eq.) and the solution stirred at 0° C. for 30 min. The solution was cooled to −78° C. and then a solution of isobutylisobutyrate (3.49 mL, 20.8 mmol) in THF (6 mL) was added dropwise and then the reaction stirred at −78° C. for 1 h. TMS-Cl (3.19 mL, 25 mmol) was then added dropwise and the reaction allowed to warm to room temperature over 3 h. The reaction was quenched with ice-water (20 mL) and EtOAc (20 mL) was added. The organic phase was washed with water (10 mL) and then brine (10 mL) before it was dried (MgSO4), filtered and concentrated to give (1-isobutoxy-2-methyl-propenyloxy)-trimethyl-silane (3.5 g) used crude in the next reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09145354B2
出典データセットuspto-grants-2015_09
ORD IDord-0a0157e6eee140748b6d58787acb1562
出典メモuspto-grants-2015_09