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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829902Generated: October 26, 2026

Water → Ethyl 3-[(trimethylsilyl)oxy]but-2-enoate

https://huagongshe.com/reaction/1829902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetoacetateHCID 8868—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductEthyl 3-[(trimethylsilyl)oxy]but-2-enoateHCID 54340571106.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

182.21 g (1.4 mol) of ethyl acetoacetate and 169.98 g (1.4 mol) of triethylamine were dissolved in a mixed solvent of 182 mL of tetrahydrofuran and 1.64 L of hexane under nitrogen atmosphere. To this solution, 167.3 g (1.54 mol) of trimethylsilyl chloride was added dropwise at a temperature of 21 to 45° C., and then the solution was stirred at 25° C. for 3 hours. The reaction mixture was cooled to 10° C., the reaction was ceased by adding 547 mL of water thereto and an organic layer was separated. The organic layer was washed two times with 273 mL of water, dried over 54.7 g of anhydrous magnesium sulfate, and then filtered. The solvent was evaporated to obtain 301.3 g (crude yield 106.4%) of 3-(trimethylsilyloxy) but-2-enoic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064209B2
Source datasetuspto-grants-2006_06
ORD IDord-b421707507ed498d8d871748c38273a5
Source noteuspto-grants-2006_06