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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505665Generated: October 30, 2026

Chlorotrimethylsilane → 1-Ethoxy-1,3-bis(trimethylsiloxy)hexa-1,3-diene

https://huagongshe.com/reaction/505665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantEthyl 3-oxohexanoateHCID 238498—
ReactantSodium BicarbonateHCID 516892—
ReactantLithium diisopropylamide mono(tetrahydrofuran)HCID 10997623—
CatalystChlorotrimethylsilaneHCID 6397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product1-Ethoxy-1,3-bis(trimethylsiloxy)hexa-1,3-dieneHCID 72952699193.6%

Reaction Steps

3-Oxohexanoic acid ethyl ester (20 mL, 0.13 mol) was dissolved in toluene (100 mL), and the obtained solution was added with triethylamine (28 mL, 0.20 mol) and chlorotrimethylsilane (24 mL, 0.19 mmol), followed by stirring at a room temperature for 4 hours. The reaction mixture was added with hexane (200 mL) and 0.5 mol/L aqueous sodium hydrogencarbonate solution and then, extracted with hexane 3 times. The organic layers were combined, sequentially washed with saturated aqueous sodium hydrogencarbonate solution and saturated brine, dried over anhydrous sodium sulfate, and then evaporated under reduced pressure. The residue was dissolved in tetrahydrofuran (100 mL) and cooled to −78° C. The obtained solution was added with 2.0 mol/L lithiumdiisopropylamide-tetrahydrofuran solution (78 mL, 0.16 mol) followed by stirring at −78° C. for 1 hour. Then, chlorotrimethylsilane (18 mL, 0.14 mol) was added and the reaction mixture was stirred at −78° C. for 8 hours. The reaction mixture was further added with hexane (200 mL) and water and extracted with hexane 3 times. The organic layers were combined, sequentially washed with saturated aqueous sodium hydrogencarbonate solution and saturated brine, dried over anhydrous sodium sulfate, and then evaporated under reduced pressure to obtain 1-ethoxy-1,3-bis(trimethylsiloxy)hexa-1,3-diene (41 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781485B2
Source datasetuspto-grants-2010_08
ORD IDord-efa76df7b0e348cfbe60ef2dc66a09fe
Source noteuspto-grants-2010_08