HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759968Generated: October 28, 2026
Phenylacetonitrile → HCID 22599823, compound
https://huagongshe.com/reaction/1759968
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Chloro-6-(methylsulfanyl)pyrimidine | HCID 21813077 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22599823 | HCID 22599823 | 81.4% |
Reaction Steps
In 30 ml of tetrahydrofuran was suspended 5.24 g of potassium t-butoxide, to which 2.63 g of phenylacetonitrile and 3.0 g of 4-chloro-6-methylthiopyrimidine, followed by stirring at 0° C. for 4 hours. The reaction mixture was then poured into a saturated aqueous ammonium chloride solution and extracted three times with ethyl acetate. The organic layers were combined and washed with a saturated aqueous sodium chloride solution, and the combined organic layer was dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography to give 3.67 g of 4-(α-cyanobenzyl)-6-methylthiopyrimidine.
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-9ee5b8655b7d47af9a80ad045076640d |
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| Source note | uspto-grants-2005_01 |
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