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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583652Generated: November 1, 2026

Butyl iodide → HCID 13535694, compound

https://huagongshe.com/reaction/1583652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantPotassium hydrideHCID 82127—
ReactantN-[(4-chlorophenyl)methyl]-(5-pyrimidyl)amineHCID 13535693—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13535694HCID 13535694—

Reaction Steps

To a solution of 2.2 g of N-[(4-chlorophenyl)methyl]-(5-pyrimidyl)amine dissolved in 50 ml of tetrahydrofuran was added 2 g of a 24.6% suspension of potassium hydride in oil. The reaction was allowed to stir at room temperature for approximately 1 hour at which time 2 g of iodobutane was added to the reaction mixture. The mixture was stirred at room temperature overnight and concentrated under reduced pressure. The residue was dissolved in diethyl ether and the organic phase was washed with water, separated and dried over anhydrous magnesium sulfate. Following concentration of the solution under reduced pressure the residue was chromatographed over silica gel. Fractions containing the major component were combined and the solvent was evaporated therefrom to afford N-butyl-N-[(4-chlorophenyl)methyl]-(5-pyrimidyl)amine as a solid. mp=67°-68° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04552960
Source datasetuspto-grants-1985_11
ORD IDord-e46af3dc58704366b0afd0bbd0b210fe
Source noteuspto-grants-1985_11