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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291205Generated: October 31, 2026

Ethanol → 7-(4-(4-Chlorobenzoyl)benzyl)-2,6-diethoxypurine

https://huagongshe.com/reaction/1291205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium ethoxideHCID 2723922—
Reactant7-(4-(4-Chlorobenzoyl)benzyl)-2,6-dichloropurineHCID 18918840—
SolventWaterHCID 962—
Product7-(4-(4-Chlorobenzoyl)benzyl)-2,6-diethoxypurineHCID 1891896967%

Reaction Steps

To a solution of 7-(4-(4-chlorobenzoyl)benzyl)-2,6-dichloropurine (1.12 g) in ethanol (30 ml) was added sodium ethoxide (1.83 g) and the mixture was stirred at room temperature for 96 hours. This reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with saturated aqueous NaCl solution and dried over anhydrous sodium sulfate and the solvent was distilled off. The residue was washed with ether and hexane to provide the title compound (0.78 g, 67%) as colorless powder. 1H-NMR (CDCl3) δ: 1.34(3H,t,J=7.OHz), 1.50(3H,t,J=7.OHz), 4.50(2H,q,J=7.OHz), 4.55(2H,q,J=7.OHz), 5.53(2H,s), 7.25-7.80(8H,m), 7.98(1H,s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753664
Source datasetuspto-grants-1998_05
ORD IDord-9e8f4277d9f64b7f9d09d65a429406a6
Source noteuspto-grants-1998_05