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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988143Generated: October 25, 2026

Water → 5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acid

https://huagongshe.com/reaction/988143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridiniumtribromideHCID 21124087—
Reactant5-(1H-indol-4-yl)-nicotinic acidHCID 22135477—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Solventtert-ButanolHCID 6386—
Product5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acidHCID 2213539798%

Reaction Steps

Pyridinium tribromide (90% (Aldrich), 9.8 g, 27.6 mmol) was added portion-wise over 10 minutes to a suspension of 5-(1H-indol-4-yl)-nicotinic acid (2.2 g, 9.2 mmol) in 2-methyl-2-propanol (54 mL), ethanol (36 mL) and acetic acid (108 mL). The mixture was stirred at room temperature for 2 hours and then acetic acid (10 mL) was added. After stirring for an additional hour, water (0.5 mL) and zinc dust (6 g, 92 mmol) were added and stirring was continued for another hour. Residual zinc dust was filtered and washed with methanol. The filtrate was concentrated and the syrupy residue was stirred in water (300 mL) overnight. The solid which formed was filtered, washed with water to remove zinc and pyridine salts and dried under high vacuum to give 2.3 g (98%) of 5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06635640B2
Source datasetuspto-grants-2003_10
ORD IDord-4f0f685df7fb4da1ba4fe72076fc25ec
Source noteuspto-grants-2003_10