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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22285Generated: October 28, 2026

Ethyl 1-oxo-2,3-dihydro-1H-pyrrolo[1,2-a]indole-2-carboxylate → 2,3-Dihydro-1H-pyrrolo[1,2-a]indol-1-one

https://huagongshe.com/reaction/22285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-oxo-2,3-dihydro-1H-pyrrolo[1,2-a]indole-2-carboxylateHCID 12582025—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2,3-Dihydro-1H-pyrrolo[1,2-a]indol-1-oneHCID 10559092—

Reaction Steps

A solution of 2,3-dihydro-1-oxo-2-ethoxycarbonyl-1H-pyrrolo[1,2-a]indole in 400 mL of acetic acid and 25 mL of water was heated at reflux under N2 for 16 hr. The resulting solution was cooled and concentrated to dryness. The residue was treated with water and methylene chloride. The organic layer was washed with NaHCO3, brine, dried and concentrated to give solid which was purified by column chromatography to give the title compound. HNMR (CDCl3)δ 2.17 (t, 2H), 4.38 (t, 2H), 6.95 (s, 1H), 7.06-7.2 (m, 1H), 7.2-7.4 (m, 2H), 7.7 (d, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428043
Source datasetuspto-grants-1995_06
ORD IDord-4935e285242f4fa0aa7aa811a5f5c13f
Source noteuspto-grants-1995_06