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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101666Generated: October 26, 2026

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

https://huagongshe.com/reaction/2101666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetoacetateHCID 8868—
SolventHexaneHCID 8058—
ProductEthyl 3-[(trimethylsilyl)oxy]but-2-enoateHCID 5434057190.9%

Reaction Steps

A solution of 31.9 mL (0.25 mole) of ethyl acetoacetate is stirred in hexane (350 mL) at room temperature. Triethylamine (42 mL, 0.30 mole) is added, followed by dropwise addition of trimethylsilyl chloride (35 mL, 0.276 mole) keeping the internal temperature below 25° C. using a water bath (about 18° C.). The thick white slurry is stirred overnight at room temperature. 200 mL of hexane is then added and the mixture stirred in an ice bath for 1 hour. The mixture is filtered and the solids are washed with 50 mL of cold hexane. Evaporation of the combined filtrate and washings gives 46 g of 3-trimethylsilanyloxy-but-2-enoic acid ethyl ester as a colorless, slightly cloudy oil. This material is used without further purification in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572917B2
Source datasetuspto-grants-2009_08
ORD IDord-6a3eff6957a94849b0da44c6bb63e0c6
Source noteuspto-grants-2009_08