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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186764Generated: October 30, 2026

Ethyl phenylacetate → HCID 10752615, compound

https://huagongshe.com/reaction/2186764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl phenylacetateHCID 7590—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-(Triphenylmethyl)pyridinium tetrafluoroborateHCID 9909412—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10752615HCID 1075261543.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl phenylacetate (3.13 g, 19 mmol, 1.0 equiv) was added in a dropwise manner to a solution of LDA (19 mmol, 1 equiv) in THF (30 mL) at −78° C. The resultant solution was maintained at to −78° C. for 25 minutes, and then warmed to 0° C. for 10 minutes. Triphenylmethylpyridinium tetrafluoroborate (7.8 g, 19 mmol, 1.0 equiv) was added in one portion. The reaction mixture was allowed to warm to 23° C. overnight and then concentrated. The residue was partitioned between saturated aqueous ammonium chloride (50 mL) and ethyl acetate (50 mL). The layers were separated, and the aqueous layer was dried over magnesium sulfate and concentrated. The residue was purified by flash column chromatography (25% THF/hexanes) to afford ethyl α-phenylpyridylacetate (2.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407120B1
Source datasetuspto-grants-2002_06
ORD IDord-471fa1d961fb4a26b588a39e6273582f
Source noteuspto-grants-2002_06