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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719882Generated: November 3, 2026

Ethyl Acetate → HCID 13220943, compound

https://huagongshe.com/reaction/1719882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-Phenyl-1-(1H-pyrrol-2-yl)ethan-1-oneHCID 13447056—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13220943HCID 13220943—

Reaction Steps

A solution of 6.00 g (0.032 mole) of the 2-phenylacetylpyrrole (III) in 200 ml of anhydrous tetrahydrofuran was added to a suspension of 600 g (0.153 mole) of lithium aluminum hydride in dry tetrahydrofuran. The mixture was stirred at reflux temperature for 48 h. The mixture was cooled to 0°, ethyl acetate was cautiously added to destroy the excess hydride and then saturated aqueous sodium sulfate was added. The organic phase was decanted, dried over sodium sulfate and evaporated in vacuo. The residue was subjected to column chromatography on neutral alumina (Fluka, Act II). 4.800 g (88%) of 2-[phenethyl]pyrrole (IV) was eluted with hexane-ethyl acetate and crystallized, m.p. 40°-42° (hexane). (Step 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04543361
Source datasetuspto-grants-1985_09
ORD IDord-5a16cb4cd35548128f009a61810779a0
Source noteuspto-grants-1985_09