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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Hydroxyethoxy)-3,5-dimethylbenzaldehydeHCID 28932578—
ReactantHCID 86659807HCID 86659807—
CatalystCupric ChlorideHCID 24014—
SolventEthanolHCID 702—
ProductHCID 46841011HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952021B2
Source datasetuspto-grants-2015_02
ORD IDord-d88a01fe356747a28a4410e98bde50b7
Source noteuspto-grants-2015_02