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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-amino-N-(4-isopropylphenyl)benzamide | HCID 2806546 | — |
| Reactant | 4-(2-Hydroxyethoxy)-3,5-dimethylbenzaldehyde | HCID 28932578 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 46841009 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952021B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-5379a414644f4ef791f40c634ade8849 |
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| Source note | uspto-grants-2015_02 |
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