HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779320Generated: October 30, 2026
Benzyl Alcohol → Benzyl 2-(4,6-dimethoxypyrimidin-2-yloxy)-6-(6-methoxypyridin-2-yl)benzoate
https://huagongshe.com/reaction/1779320
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4,6-Dimethoxy-2-(methylsulfonyl)pyrimidine | HCID 838363 | — |
| Reactant | 2,2-Dimethyl-5-(6-methoxypyridin-2-yl)-4H-(1,3)benzodioxin-4-one | HCID 15279416 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 2-(4,6-dimethoxypyrimidin-2-yloxy)-6-(6-methoxypyridin-2-yl)benzoate | HCID 15279417 | — |
Reaction Steps
1.36 g of benzyl alcohol dissolved in 50 ml of dimethylformamide are treated with 380 mg of sodium hydride (80% strength in liquid paraffin) and the mixture is subsequently stirred at room temperature for about 1 h. 3.0 g of 2,2-dimethyl-5-(6-methoxypyridin-2-yl)-4H-(1,3)benzodioxin-4-one are added, the mixture is stirred at room temperature for 3 h and 2.65 g of 4,6-dimethoxy-2-methylsulfonylpyrimidine are finally added. The mixture is stirred at room temperature for 2 h, at 80° C. for 1.5 h and at 115° C. for 3 h, poured into ice-water containing phosphoric acid and extracted with ethyl acetate, and the organic phase is washed with water, dried over sodium sulfate and concentrated under reduced pressure. The crude product is purified by chromatography on silica gel 60 using cyclohexane/toluene/ethyl acetate. 1H-NMR (CDCl3): δ=3.80(s); 3.89(s); 5.02(s); 5.72(s); 6.67(d=; 6.7-7.7(m)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05627136 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-ce1161b634e94eaba1f67255d450caf5 |
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| Source note | uspto-grants-1997_05 |
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