HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759864Generated: October 26, 2026
Potassium Carbonate → 4-(2,3-Difluorobenzyloxy)-6-(2-butynyloxy)pyrimidine
https://huagongshe.com/reaction/1759864
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,3-Difluorobenzyl Alcohol | HCID 447153 | — |
| Reactant | 4-(2-Butynyloxy)-6-methanesulfonylpyrimidine | HCID 22599863 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2,3-Difluorobenzyloxy)-6-(2-butynyloxy)pyrimidine | HCID 22599787 | 67.6% |
Reaction Steps
To 2 ml of N,N-dimethylformamide were added 0.15 g of 4-(2-butynyloxy)-6-methanesulfonylpyrimidine, 0.14 g of potassium carbonate, and 0.16 g of 2,3-difluorobenzylalcohol, followed by stirring at 50° C. for 7 hours. The reaction mixture was then left for cooling to room temperature and poured into a saturated aqueous ammonium chloride solution, which was extracted three times with chloroform. The chloroform layers were combined, washed with diluted hydrochloric acid and then with water, and dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography to give 0.13 g of 4-(2,3-difluorobenzyloxy)-6-(2-butynyloxy)pyrimidine (the present compound (76)), m.p.: 84.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06838463B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-5bd59ce27ca9431f882bbd0d60dbdba6 |
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| Source note | uspto-grants-2005_01 |
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