Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405868Generated: October 26, 2026

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

https://huagongshe.com/reaction/405868

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 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 (200 ml) was added sodium hydroxide (30.8 g, 0.77 mol). The mixture was heated to reflux for 2 hours before being cooled to room temperature and diluted with water (2.64 L). The mixture was then washed with dichloromethane (2×300 ml) and the aqueous layer was acidified with concentrated hydrochloric acid to pH 1.0. The precipitate formed was collected by filtration, washed with water and dried to yield 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid as a dark yellow solid (23 g, 85%). 1H NMR (DMSO-d6) 400 MHz δ: 11.95 (brs, 1H), 7.96 (s, 1H), 7.69 (d, 1H, J=8.4 Hz), 7.06 (t, 1H, J=6.8 Hz), 6.92 (d, 1H, J=6.8 Hz), 4.19 (t, 2H, J=6 Hz), 2.91 (t, 2H, J=6 Hz), 2.11 (t, 2H, J=5.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754078B2
Source datasetuspto-grants-2014_06
ORD IDord-8d9d2c6e8b8a4f7093f1f2416fa9dac9
Source noteuspto-grants-2014_06