HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 7-(4-(4-Chlorobenzoyl)benzyl)-2,6-diethoxypurine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 7-(4-(4-Chlorobenzoyl)benzyl)-2,6-dichloropurine | HCID 18918840 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-(4-(4-Chlorobenzoyl)benzyl)-2,6-diethoxypurine | HCID 18918969 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753664 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-9e8f4277d9f64b7f9d09d65a429406a6 |
| Source note | uspto-grants-1998_05 |