Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N,N-Diethylaniline | HCID 7061 | — |
| Reactant | HCID 18999461 | HCID 18999461 | — |
| Product | HCID 15278457 | HCID 15278457 | — |
Reaction Steps
In 100 ml of N,N-diethylaniline, 8.0 g of 1-(3-allyloxy-4-chlorophenyl)-3-methyl-4-trifluoromethyl-1,2,3,6-tetrahydropyrimidine-2,6-dione was dissolved, and the solution was stirred at 180° C. for 3 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and poured into diluted hydrochloric acid. The mixture was extracted with ethyl acetate. The organic layer was washed with water, dried and concentrated. The residue was purified by silica gel chromatography, which afforded 6.3 g of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05476834 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-bab351ad2e9445feb307a1aac75d6f62 |
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| Source note | uspto-grants-1995_12 |
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