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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820132Generated: October 30, 2026

Water → HCID 68712205, compound

https://huagongshe.com/reaction/1820132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,5-Dimethyl-4-nitroanilineHCID 36911—
Reactant4-(Trifluoromethyl)benzaldehydeHCID 67996—
SolventEthanolHCID 702—
ProductHCID 68712205HCID 6871220585%

Reaction Steps

3,5-Dimethyl-4-nitro-phenylamine (3.95 g) and 4-trifluoromethyl-benzaldehyde (4.87 mL) were dissolved in ethanol (50 mL) and refluxed for 16 h. The reaction mixture was poured into water (75 mL) and the precipitate collected by filtration. Sodium cyanoborohydride (3.1 g) and acetic acid (7.0 mL) were added to the precipitate dispersed in methanol (130 mL) and stirred for 60 minutes. The reaction mixture was filtered, water (350 mL) was added and the organic solvent was removed in vacuo. The product was allowed to precipitate at 25° C. and collected by filtration and washed with water (300 mL) to furnish 6.7 g (85% yield) of the title compound as a yellow solid. LC-MS (m/z) 325 (MH+); tR=2.00, (UV, ELSD) 92%, 93%. 1H NMR (500 MHz, CDCl3): 2.30 (s, 6H), 4.45 (broad, 3H), 6.25 (s, 2H), 7.45 (d, 2H), 7.60 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601870B2
Source datasetuspto-grants-2009_10
ORD IDord-30900ba695774559a9b4c8f9519664d4
Source noteuspto-grants-2009_10