HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129469Generated: November 1, 2026
N,N-Diethylaniline → 4-Chloro-5-nitro-6-ethylpyrimidine
https://huagongshe.com/reaction/129469
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Diethylaniline | HCID 7061 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | HCID 178437745 | HCID 178437745 | — |
| Product | 4-Chloro-5-nitro-6-ethylpyrimidine | HCID 19371729 | — |
Reaction Steps
18.7 g (0.125 mol) of diethylaniline are dissolved in 18 ml of phosphorus chloride, and then 8.46 g (0.05 mol) of 4-hydroxy-5-nitro-6-ethylpyrimidine are stirred in. During the addition, the temperature rises from 22° to 47° C. A solution is formed which is heated at 60° C. for 2 hours. It is then stirred with ice-water and ethyl acetate for 30 minutes for the purpose of hydrolysis. The organic phase is separated off and combined with the extracts obtained by extraction, and the mixture is washed with NaHCO3 solution. Removal of the solvent yields 9.1 g of crude product, which is purified by column chromatography on silica gel (eluant:ethyl acetate/hexane 20:80 parts). 6.76 g (72.1% of the theoretical yield) of pure product are obtained in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05468751 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-dd2d483ddd3848d0a51cb0cc84f50dc8 |
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| Source note | uspto-grants-1995_11 |
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