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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741719Generated: November 1, 2026

HCID 18963910, compound → HCID 18963936, compound

https://huagongshe.com/reaction/1741719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18963910HCID 18963910—
SolventEthanol hydrochlorideHCID 21887872—
ProductHCID 18963936HCID 18963936—

Reaction Steps

2-(3-Phenylpropyl)-5-methoxy-3-hydroxy-1-oxo-1,3-dihydrobenzo[c]pyrrole (2.49 g, 8.38 mmol) is dissolved in HCl/EtOH (50 ml concentrated HCl, 150 ml EtOH), and N2 is bubbled through the solution for 10 minutes followed by the addition of the catalyst, 10% Pd/C (200 mg). The mixture is hydrogenated on a Parr-Shaker apparatus at 3 atmospheres pressure for 3 hours. After filtering the reaction through a pad of Celite, the filtrate is concentrated in vacuo, and the residue is dissolved in EtOAc (200 ml). The EtOAc is washed with 2N HCl (200 ml), H2O (200 ml), saturated NaHCO3 solution (200 ml) and saturated NaCl solution (200 ml) dried over MgSO4 and evaporated. The product is purified by chromatography (SiO2 ; 1:9 EtOAc/hexanes, 1:4 EtOAc/hexanes) to yield 2-(3-phenylpropyl)-5-methoxy-1-oxo-1,3-dihydrobenzo[c]pyrrole. Treatment with BBr3 yields 2-(3-phenylpropyl)-5 -hydroxy-1-oxo-1,3-dihydrobenzo[c]pyrrole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334600
Source datasetuspto-grants-1994_08
ORD IDord-11d4fa2b82b248feaf12c2591ae602ba
Source noteuspto-grants-1994_08