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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2283430Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2283430

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
EduktIsobutyl isobutyrateHCID 7351—
EduktDiisopropylamineHCID 7912—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(1-Isobutoxy-2-methyl-propenyloxy)-trimethyl-silaneHCID 1562627677,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09145354B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-0a0157e6eee140748b6d58787acb1562
Quellennotizuspto-grants-2015_09