HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 4-Amino-2-benzyl-5-phenylazopyrimid-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzenediazonium chloride | HCID 60992 | — |
| Reactant | 6-amino-2-benzylpyrimidin-4(3H)-one | HCID 135596637 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Amino-2-benzyl-5-phenylazopyrimid-6-one | HCID 136354617 | — |
Reaction Steps
A cold solution of benzenediazonium chloride (prepared by the method well known in the art, from 2 g. aniline) was added dropwise with stirring to a solution of 4-amino-2-benzylpyrimid-6-one (4 g.) and sodium hydroxide (1.6 g.) in water (50 ml.) at 5° C. After stirring for a further 1 hour, the solid was filtered off and recrystallised from a mixture of dimethylformamide and water (4:1 v/v) to give 4-amino-2-benzyl-5-phenylazopyrimid-6-one (3.8 g.) in the form of orange needles, which decomposed at 256°-257° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03987160 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-1229000a61ef4024aaa189480fc98870 |
| Source note | uspto-grants-1976_10 |