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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731192Generated: October 25, 2026

Ethyl trimethylsilylacetate → Ethyl 3-(4-(benzyloxy)phenyl)-3-(3-methyl-3H-1,2,3-triazol-4-yl)acrylate

https://huagongshe.com/reaction/731192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trimethylsilylacetateHCID 77687—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant(4-(Benzyloxy)phenyl)(3-methyl-3H-1,2,3-triazol-4-yl)methanoneHCID 57835886—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(4-(benzyloxy)phenyl)-3-(3-methyl-3H-1,2,3-triazol-4-yl)acrylateHCID 6868752895.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of lithium bis(trimethylsilyl)amide (22 mmol, 1 M in THF) was added ethyl trimethylsilylacetate (31.5 mmol) dropwise at −78° C. After 20 minutes at −78° C., a solution of 73.3 (14.7 mmol) in THF (50 mL) was added dropwise, and the reaction was maintained at −78° C. for 4 hours. The reaction was quenched with saturated NH4Cl (aq) and warmed to room temperature. The mixture was extracted with EtOAc (500 mL), dried over anhydrous sodium sulfate, filtered, and concentrated with silica gel under reduced pressure. The residue was chromatographed (silica gel, 1:1 EtOAc/hexane) to afford compound 73.4 (5.1 g, 14 mmol). MS ESI (pos.) m/e 364.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582803B2
Source datasetuspto-grants-2009_09
ORD IDord-d3b6dc36570846d99f11717850f3a53a
Source noteuspto-grants-2009_09