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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351571Generated: October 25, 2026

Sodium Hydroxide → 5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid

https://huagongshe.com/reaction/351571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylateHCID 20729414—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acidHCID 2255688685%

Reaction Conditions

Temperature22 °C

Reaction Steps

To a solution of 5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid ethyl ester (31 g, 0.14 mol) in ethanol (200 mL) and water (70 mL) was added 5 N aqueous sodium hydroxide(60 mL, 0.3 mol) and the resulting mixture stirred at reflux for 3 hours. The reaction mixture was cooled to 20-24° C., diluted with water (2 L) and washed with dichloromethane(2×200 mL) and diethyl ether (1×200 mL). The aqueous layer was filtered through Celite and the filtrate was acidified with conc. HCl (25 mL) to precipitate the product. The solid was filtered, washed with water (200 mL), and dried in vacuo to give 23.2 g (85%) of the desired compound as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743785B2
Source datasetuspto-grants-2004_06
ORD IDord-bf93516ce3db42ed84e196223a0db2f6
Source noteuspto-grants-2004_06