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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477394Generated: October 30, 2026

Water → HCID 15079924, compound

https://huagongshe.com/reaction/477394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantHCID 15079923HCID 15079923—
CatalystTetrabutylphosphonium bromideHCID 76564—
SolventBenzeneHCID 241—
SolventSodium HydroxideHCID 14798—
ProductHCID 15079924HCID 1507992483.9%

Reaction Steps

Four grams N-[4-[(4,6-dimethylpyrimidin-2-yl)thio]phenyl]hexanamide, 3.4 g methyl iodide and 0.4 g tetrabutylphosphonium bromide was dissolved in a mixture of 10 ml 50% NaOH and 50 ml benzene. This was stirred vigorously at room temperature for 72 hours. Fifty milliliters water was then added and the benzene layer was separated off. The benzene solution was washed with 4×100 ml water then dried over Na2SO4. The solvent was evaporated giving 3.5 g dark brown oil. The oil was chromatographed on silica gel eluted with 50% ethyl acetate/hexanes giving 2.5 g yellow oil which slowly crystallized. Melting point of the resulting pale yellow wolid was 61°-63° C. The structure was confirmed by infrared, nuclear magnetic resonance and mass spectral analysis as that of the desired product, N-[4[(4,6-dimethylpyrimidin-2-yl)thio]phenyl]-N-methylhexanamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888047
Source datasetuspto-grants-1989_12
ORD IDord-0f37a8142f5b4e599130f56cf0da0f1b
Source noteuspto-grants-1989_12