Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246653Generated: October 26, 2026

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

https://huagongshe.com/reaction/2246653

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 4.2 (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 4.3 (2.49 g). MS ESI (pos.) m/e 357.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687526B2
Source datasetuspto-grants-2010_03
ORD IDord-532d55fecd524d19b13749931a502df0
Source noteuspto-grants-2010_03