HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847374Generated: October 25, 2026
1,3-Dimethyl-2-imidazolidinone → HCID 131717499, compound
https://huagongshe.com/reaction/847374
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | Octafluorotoluene | HCID 9906 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | DL-5 Chloro-6-ethyl-4-(alphaethyl-4-hydroxybenzylamino)pyrimidine | HCID 131716268 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131717499 | HCID 131717499 | 111.7% |
Reaction Steps
A mixture of 1 g of dl-5-chloro-6-ethyl-4-(α-ethyl-4-hydroxybenzylamino)pyrimidine, 1 g of perfluorotoluene, 0.24 g of powdery potassium hydroxide and 20 ml of 1,3-dimethyl-2-imidazolidinone (DMI) was heated under stirring at 70° C. for 8 hours. After completion of the reaction, the reaction mixture was poured into water, and extracted with toluene. The extract was washed with water, dried over anhydrous sodium sulfate and then toluene was evaporated under reduced pressure. The oily product obtained was isolated by column chromatography (Wako gel C-200, eluted with toluene:ethyl acetate=30:1) to give 1.5 g of the desired product as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05141941 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-fae56da5724e44ad83bde53adc3f8250 |
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| Source note | uspto-grants-1992_08 |
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