HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5-Ethoxycarbonyl 4-ethoxy 2-ethyl pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 4-chloro-2-ethylpyrimidine-5-carboxylate | HCID 12363083 | — |
| Product | 5-Ethoxycarbonyl 4-ethoxy 2-ethyl pyrimidine | HCID 12901692 | 68% |
Reaction Steps
To a solution cooled to 0° C. of 64.5 g of 5-ethoxycarbonyl 4-chloro 2-ethyl pyrimidine obtained in the preceding stage, in 200 ml of ethanol, was slowly added a solution of 7.75 g of sodium in 200 ml of ethanol, this being stirred for 15 min. after the addition. Then the solution was acidified to a pH≃3 with hydrochloric ethanol≃6.5 N, and the solvent was evaporated. The residue was diluted in water, extracted with chloroform, dried on sodium sulfate and the solvent evaporated. The residue was distilled and 46.7 g of the expected product were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04250178 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-34a9c3398b6d4d9db31cff6d0452648c |
| Source note | uspto-grants-1981_02 |