HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846538Generated: October 30, 2026
Water → (3-Chlorophenyl)(4,6-dimethoxypyrimidin-2-yl)acetonitrile
https://huagongshe.com/reaction/846538
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | m-Chlorophenylacetonitrile | HCID 73722 | — |
| Reactant | 4,6-Dimethoxy-2-(methylsulfonyl)pyrimidine | HCID 838363 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (3-Chlorophenyl)(4,6-dimethoxypyrimidin-2-yl)acetonitrile | HCID 19882861 | 91.1% |
Reaction Steps
Sodium hydride (6.0 g of 80% in oil) was added portionwise to a stirred solution of 4,6-dimethoxy-2-(methylsulphonyl)pyrimidine (21.8 g) and (3-chlorophenyl)acetonitrile (15.1 g) in dry dimethylformamide (150 ml) at 5° C. The mixture was stirred at 10° C. for 30 minutes, and then at room temperature for 3 hours. The resulting suspension was poured into water (1.2 l) and the oil was extracted into ether. The combined extracts were washed with saturated sodium chloride solution, dried over magnesium sulphate and evaporated to give an orange oil, which was purified by chromatography to give 26.3 g of the desired product as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05137564 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-48ecee1ddf474e8cbbe0d7537dd578ed |
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| Source note | uspto-grants-1992_08 |
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