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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283430Generated: October 27, 2026

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

https://huagongshe.com/reaction/2283430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantIsobutyl isobutyrateHCID 7351—
ReactantDiisopropylamineHCID 7912—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(1-Isobutoxy-2-methyl-propenyloxy)-trimethyl-silaneHCID 1562627677.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145354B2
Source datasetuspto-grants-2015_09
ORD IDord-0a0157e6eee140748b6d58787acb1562
Source noteuspto-grants-2015_09