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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731197Generated: October 25, 2026

Ethyl trimethylsilylacetate → Ethyl 3-(1-methyl-1H-imidazol-5-yl)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)acrylate

https://huagongshe.com/reaction/731197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trimethylsilylacetateHCID 77687—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant(1-Methyl-1H-imidazol-5-yl)(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)methanoneHCID 57835849—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(1-methyl-1H-imidazol-5-yl)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)acrylateHCID 68686278118.4%

Reaction Conditions

Temperature-45 °C

Reaction Steps

To a solution of lithium bis(trimethylsilyl)amide (6.8 mmol, 1 M in THF) was added ethyl trimethylsilylacetate (6.5 mmol) dropwise at −78° C. After 20 minutes at −78° C., a solution of 74.2 (5.9 mmol) in THF (20 mL) was added dropwise. The reaction was maintained at −78° C. for 3 hours and at −45° C. for 2 hours. The reaction was quenched with saturated NH4Cl (aq) at 0° C. and warmed to room temperature. The mixture was extracted with EtOAc (500 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to afford crude 74.3 (2.49 g). MS ESI (pos.) m/e 357.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582803B2
Source datasetuspto-grants-2009_09
ORD IDord-d76b189b63724601a6cd10248700550d
Source noteuspto-grants-2009_09