HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413436Generated: November 2, 2026
Phosphorus oxychloride → Ethyl 4-chloro-2-ethylpyrimidine-5-carboxylate
https://huagongshe.com/reaction/1413436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178469771 | HCID 178469771 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 4-chloro-2-ethylpyrimidine-5-carboxylate | HCID 12363083 | — |
Reaction Steps
7.5 ml of triethylamine were slowly introduced into 300 ml of phosphorous oxychloride cooled to 0° C., then were added 30 g of 5-ethoxycarbonyl 4-hydroxy 2-ethyl pyrimidine (VII) prepared in the preceding stage and the suspension was brought up to 40° C. under nitrogen scavenging. After dissolution, the phosphorous oxychloride was evaporated and the residue diluted in a mixture of water and chloroform. This was decanted, the chloroform phase was twice washed with water, dried on sodium sulfate and the solvent evaporated. The raw product obtained, after checking the purity by thin layer chromatography, was reacted in the following stage 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04250178 |
|---|
| Source dataset | uspto-grants-1981_02 |
|---|
| ORD ID | ord-ffd9be3dd206450d9b6d8d96b70394b1 |
|---|
| Source note | uspto-grants-1981_02 |
|---|