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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736053Generated: October 25, 2026

Nitroethane → 6-fluoro-3-(2-nitropropenyl)-1H-indole

https://huagongshe.com/reaction/736053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitroethaneHCID 6587—
Reactant6-Fluoroindole-3-carboxaldehydeHCID 262903—
ReactantAmmonium AcetateHCID 517165—
SolventEthyl AcetateHCID 8857—
Product6-fluoro-3-(2-nitropropenyl)-1H-indoleHCID 6664051286%

Reaction Steps

6-Fluoro-3-(2-nitropropenyl)-1H-indole was prepared by combining 6-fluoroindole-3-carboxaldehyde (485 mg, 2.97 mmol), nitroethane (6.0 mL), and ammonium acetate (250 mg, 3.27 mmol). The reaction solution was allowed to reflux 2 hours. The reaction solution was diluted with EtOAc (100 mL), washed with H2O (50 mL×2), partitioned, dried over Na2SO4, filtered, and concentrated under reduced pressure to provide 560 mg (86% yield) of 6-fluoro-3-(2-nitropropenyl)-1H-indole; 1H NMR (CDCl3) δ 11.03 (1H, br s), 8.41 (1H, s), 7.63 (1H, dd), 7.50 (1H, s), 7.06 (1H, dd), 6.92 (1H, t), 2.44 (3H, s); TLC (SiO2 plate, 100% DCM) Rf=0.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595311B2
Source datasetuspto-grants-2009_09
ORD IDord-5d5ecefe724541e3943875e34de114ca
Source noteuspto-grants-2009_09