Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054707Generated: November 2, 2026

Isopropylamine → N-Isopropyl-2-nitroaniline

https://huagongshe.com/reaction/2054707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductN-Isopropyl-2-nitroanilineHCID 1058351896.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold solution of 2-fluoro-nitrobenzene (31.8 g, 0.225 mol) in ethanol (300 mL) cooled in an ice bath was added isopropylamine (54.0 mL, 0.634 mol), followed by the addition of a solution of potassium carbonate (31.1 g, 0.225 mol) in water (120 mL). The mixture was stirred at 0° C. for 1 h, then refluxed for 6 h. The reaction was terminated by cooling the mixture to ambient temperature, and evaporating it under reduced pressure yielding an orange residue. The residue was partitioned between ethyl ether (800 mL) and a brine solution (300 mL). The organic layer was dried and filtered, to provide the title intermediate (39 g) as an orange liquid. 1H-NMR (CDCl3, 300 MHz): δ (ppm) 8.06 (d, 1H), 7.30 (t, 1H), 6.74 (d, 1H), 6.48 (t, 1H), 3.73 (hept, 1H), 1.20(d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329752B2
Source datasetuspto-grants-2008_02
ORD IDord-3297dfc862a14ff68b9459a34062dee0
Source noteuspto-grants-2008_02