HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703864Generated: October 30, 2026
Water → DL-5 Chloro-6-ethyl-4-(alpha-ethyl-4-acetonyloxybenzyl)aminopyrimidine
https://huagongshe.com/reaction/703864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | DL-5 Chloro-6-ethyl-4-(alphaethyl-4-hydroxybenzylamino)pyrimidine | HCID 131716268 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | DL-5 Chloro-6-ethyl-4-(alpha-ethyl-4-acetonyloxybenzyl)aminopyrimidine | HCID 131716273 | 39.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04985426 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-9cbdc0db2e91416189d55fe98d5d1109 |
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| Source note | uspto-grants-1991_01 |
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