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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759968Generated: October 28, 2026

Phenylacetonitrile → HCID 22599823, compound

https://huagongshe.com/reaction/1759968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetonitrileHCID 8794—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Chloro-6-(methylsulfanyl)pyrimidineHCID 21813077—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22599823HCID 2259982381.4%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838463B2
Source datasetuspto-grants-2005_01
ORD IDord-9ee5b8655b7d47af9a80ad045076640d
Source noteuspto-grants-2005_01