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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846308Generated: November 1, 2026

2-amino-N-(4-isopropylphenyl)benzamide → HCID 46841009, compound

https://huagongshe.com/reaction/1846308

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-amino-N-(4-isopropylphenyl)benzamideHCID 2806546—
Reactant4-(2-Hydroxyethoxy)-3,5-dimethylbenzaldehydeHCID 28932578—
CatalystCupric ChlorideHCID 24014—
SolventEthanolHCID 702—
ProductHCID 46841009HCID 46841009—

Reaction Steps

To a solution of 2-amino-N-(4-isopropylphenyl)benzamide (0.400 g, 1.57 mmol) and 4-(2-hydroxyethoxy)-3,5-dimethylbenzaldehyde (0.30 g, 1.57 mmol) in anhydrous ethanol (20 mL) was added anhydrous copper (II) chloride (0.63 g, 4.71 mmol). The reaction mixture was stirred at reflux for 4 hours under nitrogen. The solvent was removed and the residue was diluted with dichloromethane (150 mL) and water (100 mL). The organic phase was separated and further washed with water (100 mL), brine (100 mL), and dried over sodium sulfate. The crude mixture was purified by column chromatography on silica gel (230-400 mesh) using hexane/ethyl acetate (1:1) as eluent to give the title compound as a white solid. Yield: 100 mg (15.6%). MP 160-162° C. 1H-NMR (400 Hz, CDCl3): δ 8.34 (d, J=7.6 Hz, 1H), 7.80 (m, 2H), 7.52 (m, 1H), 7.17 (d, J=8.4 Hz, 2H), 7.05 (d, J=8.4 Hz, 2H), 6.97 (s, 2H), 3.90 (m, 2H), 3.78 (t, J=4.8 Hz, 2H), 2.86 (m, 1H), 2.13 (s, 6H), 2.06 (t, J=6.4 Hz, 1H), 1.20 (d, J=7.2 Hz, 3H). MS (ES+) m/z: 429.52 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952021B2
Source datasetuspto-grants-2015_02
ORD IDord-5379a414644f4ef791f40c634ade8849
Source noteuspto-grants-2015_02