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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410285Generated: October 28, 2026

Hydrochloric Acid → 1-N,1-N-diethyl-4-(trifluoromethyl)benzene-1,2-diamine

https://huagongshe.com/reaction/2410285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStannous ChlorideHCID 24479—
ReactantSodium BicarbonateHCID 516892—
ReactantN,N-Diethyl-2-nitro-4-(trifluoromethyl)anilineHCID 23149637—
SolventMethanolHCID 887—
Product1-N,1-N-diethyl-4-(trifluoromethyl)benzene-1,2-diamineHCID 496217164.8%

Reaction Steps

Concentrated hydrochloric acid (1.00 ml, 12.0 mmol) and anhydrous tin dichloride (908 mg, 4.78 mmol) were sequentially added at 0° C. to a methanol (5 ml) solution of 1-diethylamino-2-nitro-4-(trifluoromethyl)benzene (251 mg, 0.957 mmol), obtained as described in Referential Example 6-1. The resulting mixture was warmed to room temperature and stirred for 22 hours. A saturated solution of sodium hydrogen carbonate was added to the mixture, and the resulting mixture was extracted three times with ethyl acetate. The obtained organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (20 g, hexane/ethyl acetate=20/1-10/1). Thus, 2-amino-1-diethylamino-4-(trifluoromethyl)benzene (144 mg, 64.7%) was yielded as a colorless oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816089B2
Source datasetuspto-grants-2014_08
ORD IDord-858d922141b04e34a3c19fc4e37a9fd4
Source noteuspto-grants-2014_08