HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Benzaldehyde, 4-(diphenylamino)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Hydrazine, 1,1-diphenyl-, hydrochloride (1:1) | HCID 10738 | — |
| Product | Benzaldehyde, 4-(diphenylamino)- | HCID 77846 | 200% |
Reaction Steps
To a 300 ml four-neck flask were added 17.0 g (77 mmol) of 1,1-diphenylhydrazine hydrochloride obtained in Comparative Example 2, 21.1 g (77 mmol) of p-diphenylaminobenzaldehyde, and 70 g of DMF, followed by stirring at 40 to 45° C. for 3 hours. The reaction was traced by thin-layer chromatography. After, the completion of the reaction, 100 g of methanol was added and precipitated crystals were filtered off to obtain 32.3 g of p-diphenylaminobenzaldehyde=diphenylhydrazone. The yield was 95.4% based on the starting 1,1-diphenylhydrazine, the over all yield from the starting diphenylamine was 77.0%, and the purity determined by high-performance liquid chromatography was 98.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07884245B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-427df1b4d7f440dc8d52b2412bea92ee |
| Source note | uspto-grants-2011_02 |