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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502146Generated: October 31, 2026

Water → 5-Nitroindole

https://huagongshe.com/reaction/502146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-NitroindoleHCID 22523—
SolventPyridineHCID 1049—
Product5-NitroindoleHCID 22523272.3%
Product3-Bromo-5-nitro-1H-indoleHCID 43152084—

Reaction Steps

To a solution of 5-nitroindole (5.00 g, 30.8 mmol) in pyridine (200 mL) at −4° C. is added a solution of pyridinium bromide perbromide (10.99 g, 34.3 mmol) in pyridine (200 mL) dropwise under nitrogen with stirring. After complete addition, the reaction mixture is stirred for 5 min at 0° C. The reaction mixture is diluted in 0° C. water (200 mL) and extracted with 200 mL of Et2O. The organic layer is washed with 6 M HCl (300 mL), 5% NaHCO3 (300 mL), and brine (300 mL). The organic phase is dried over MgSO4 and solvent is removed to give 3-bromo-5-nitroindole as a yellow powder, 80% pure with 20% 5-nitroindole (6.80 g, 74% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772271B2
Source datasetuspto-grants-2010_08
ORD IDord-a66abff69f794ea9b92b5fdda6206694
Source noteuspto-grants-2010_08