HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzaldehyde → HCID 53983876, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Methylpyrimidine | HCID 18922 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53983876 | HCID 53983876 | 77% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
The starting compound is prepared as follows. p-Nitrobenzaldehyde (24.2 g), 4-methyl-pyrimidine (15.5 g) and acetic anhydride (16.7 g) are mixed at room temperature, and the mixture is heated at 120° C. for 5 hours. After cooling, the mixture is poured into water (500 ml), and the aqueous mixture is extracted several times with chloroform. The combined chloroform extracts are dried over magnesium sulfate and concentrated until crystals separated. Addition of ether gives 4-[2-(p-nitrophenyl)ethenyl]pyrimidine (28 g), m.p. 213°-215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04681884 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-384f58d0299f4858a983b6baee5b5b37 |
| Source note | uspto-grants-1987_07 |