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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330316Generated: October 31, 2026

Water → DL-5 Chloro-6-ethyl-4-(alpha-ethyl-4-acetonyloxybenzyl)aminopyrimidine

https://huagongshe.com/reaction/330316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroacetoneHCID 6571—
ReactantPotassium CarbonateHCID 11430—
ReactantDL-5 Chloro-6-ethyl-4-(alphaethyl-4-hydroxybenzylamino)pyrimidineHCID 131716268—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductDL-5 Chloro-6-ethyl-4-(alpha-ethyl-4-acetonyloxybenzyl)aminopyrimidineHCID 13171627339.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3.0 g of dl-5-chloro-6-ethyl-4-(α-ethyl-4-hydroxybenzyl)aminopyrimidine dissolved in 30 ml of N,N-dimethylformamide were added 1.2 g of chloroacetone and 1.7 g of anhydrous potassium carbonate, and the mixture was stirred at 80° C. for 8 hours. After completion of the reaction, the reaction mixture was charged into water and the separated oily product was extracted with ethyl acetate. The extract was washed with water, dried with anhydrous sodium sulfate, and then ethyl acetate was distilled off under reduced pressure. The oily product obtained was isolated by column chromatography (Wako Gel C-200, trade name, eluted with toluene: ethyl acetate=7:1) to give 1.3 g of the desired product as pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04895849
Source datasetuspto-grants-1990_01
ORD IDord-5d5a1da1b12146dfb5beb5e0310039f4
Source noteuspto-grants-1990_01