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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099585Generated: October 25, 2026

Methyl phenylacetate → Methyl 2-(1-benzylpyrrolidin-2-ylidene)(phenyl)acetate

https://huagongshe.com/reaction/2099585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl phenylacetateHCID 7559—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-benzyl-5-ethoxy-3,4-dihydro-2H-pyrrolium tetrafluoroborateHCID 86602992—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(1-benzylpyrrolidin-2-ylidene)(phenyl)acetateHCID 68800975—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Lithium hexamethyldisilazide solution (8.39 mL of 1M in tetrahydrofuran, 8.39 mmol) was added to dry THF and cooled to −78° C. Methyl phenylacetate (1.15 mL, 7.99 mmol) was added dropwise, and the reaction stirred for 15 minutes. A solution of 1-benzyl-5-ethoxy-3,4-dihydro-2H-pyrrolium tetrafluoroborate in 5 mL of tetrahydrofuran was added dropwise, and after one hour the reaction was allowed to warm to room temperature. The mixture was quenched with saturated NaHCO3 solution, warmed to ambient temperature and poured into water. The aqueous layer was extracted with EtOAc and the organic extract was washed with brine, dried with Na2SO4, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography (25-30% EtOAc/hexane), providing methyl 2-(1-benzylpyrrolidin-2-ylidene)(phenyl)acetate. ESI+MS: 308.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569589B2
Source datasetuspto-grants-2009_08
ORD IDord-df6d0ed43c554512bdff51d82061937b
Source noteuspto-grants-2009_08