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HRID 2283430생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2283430

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물Isobutyl isobutyrateHCID 7351—
반응물DiisopropylamineHCID 7912—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(1-Isobutoxy-2-methyl-propenyloxy)-trimethyl-silaneHCID 1562627677.8%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09145354B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-0a0157e6eee140748b6d58787acb1562
출처 메모uspto-grants-2015_09