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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440916Generated: October 30, 2026

Trifluoroacetic acid → N1-isopropyl-4-chloro-2-nitroaniline

https://huagongshe.com/reaction/440916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2,2-DimethoxypropaneHCID 6495—
Reactant4-Chloro-2-nitroanilineHCID 6979—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
SolventEthyl acetate hexaneHCID 21226206—
ProductN1-isopropyl-4-chloro-2-nitroanilineHCID 273669278.3%

Reaction Steps

4-chloro-2-nitroaniline (8.6 g; 0.05 mole), 2,2-dimethoxypropane (10.0 ml; 0.9 mole) and trifluoroacetic acid [TFA] (4.0 ml; 0.005 moles) were dissolved in toluene (100 ml) and stirred for 1 hr. BH3 pyridine (5.0 ml; 0.05 moles) was added in 1.0 ml increments. The reaction was exothermic, and the reaction progress was monitored by tlc 40%EtOAc/Hexane. Additional TFA, BH3 * pyridine and 2,2-dimethoxypropane were added until the tlc indicated that the 4-chloro-2-nitroaniline was consumed. The reaction mixture was placed on a bed of silica and eluted with toluene. The product was the first major component to elute, which produced 8.4 g (78%) of a yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521193
Source datasetuspto-grants-1996_05
ORD IDord-c7df2b0721a44929929313158bf63922
Source noteuspto-grants-1996_05