HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl (ethoxymethylene)malonate → HCID 21388814, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 15564093 | HCID 15564093 | — |
| Reactant | HCID 54377863 | HCID 54377863 | — |
| Reactant | HCID 178440774 | HCID 178440774 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21388814 | HCID 21388814 | — |
Reaction Steps
The starting material can be obtained according to the procedure of A. R. Todd and F. Bergel, J. Chem. Soc. 1937, 366 from p-n-butylbenzamidine hydrochloride and ethoxymethylenemalonic acid diethyl ester with sodium ethylate in ethanol and subsequent treatment of the obtained 2-(p-n-butylphenyl)-4-hydroxy-5-pyrimidinecarboxylic acid ethyl ester (melting point 198.0°-198.8° C) with phosphorus oxychloride. The melting point of 2-(p-n-butylphenyl)-4-chloro-5-pyrimidinecarboxylic acid ethyl ester is 64.9°-65.3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03997536 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-27a12a40276a476dae78f6a968dd7a00 |
| Source note | uspto-grants-1976_12 |