HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846315Generated: November 3, 2026
4-(2-Hydroxyethoxy)-3,5-dimethylbenzaldehyde → HCID 46841011, compound
https://huagongshe.com/reaction/1846315
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(2-Hydroxyethoxy)-3,5-dimethylbenzaldehyde | HCID 28932578 | — |
| Reactant | HCID 86659807 | HCID 86659807 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 46841011 | HCID 46841011 | — |
Reaction Steps
To a solution of 2-amino-N-(4-bromophenyl)-3-chlorobenzamide (0.52 g, 1.60 mmol) and 4-(2-hydroxyethoxy)-3,5-dimethylbenzaldehyde (0.31 g, 1.60 mmol) in anhydrous ethanol (20 mL), anhydrous copper (II) chloride (0.86 g, 6.40 mmol) was added and the reaction mixture was refluxed for 16 hours. The solvent was evaporated in vacuo, water (100 mL) was then added, and the product was extracted with ethyl acetate (200 mL). The organic phase was separated, washed with water (2×100 mL), then brine (100 mL), and dried over anhydrous Na2SO4. The solvent was evaporated, and the crude compound was purified by the Simpliflash system (20-40% ethyl acetate in hexanes as eluent), to give the title compound as a white solid. Yield 0.37 g (46%). MP 185-186° C. 1H-NMR (400 MHz, CDCl3) 8.25 (d, J=8.20 Hz, 1H) 7.89 (d, J=7.42 Hz, 1H) 7.56-7.34 (m, 3H) 7.03 (t, J=4.29 Hz, 4H), 4.06-3.87 (m, 2H) 3.87-3.74 (m, 2H) 2.18 (s, 6H) 2.11-1.95 (m, 1H). MS (ES+) m/z: 499.36, 501.38 (100%), 503.33.
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-d88a01fe356747a28a4410e98bde50b7 |
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| Source note | uspto-grants-2015_02 |
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