HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl (ethoxymethylene)malonate → HCID 21388834, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Benzamidine, p-butoxy-, monohydrochloride | HCID 3015453 | — |
| Reactant | HCID 3614036 | HCID 3614036 | — |
| Reactant | HCID 178450108 | HCID 178450108 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21388834 | HCID 21388834 | — |
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 a p-n-butoxybenzamidine hydrochloride and ethoxymethylenemalonic acid diethyl ester with sodium ethylate in ethanol and subsequent treatment of the obtained 2-(p-n-butoxyphenyl)-4-hydroxy-5-pyrimidinecarboxylic acid ethyl ester (melting point 219.0°-220.0° C) with phosphorus oxychloride. The melting point of 2-(p-n-butoxyphenyl)-4-chloro-5-pyrimidinecarboxylic acid ethyl ester is 81.0°-81.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04066570 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-f4cca56a04854e58a3a110734f8e67ac |
| Source note | uspto-grants-1978_01 |