HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Dimethylamino)Benzaldehyde → HCID 15219578, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Dimethylamino)Benzaldehyde | HCID 7479 | — |
| Reactant | 1,4-Dimethylpyridin-1-ium iodide | HCID 200603 | — |
| Reactant | Sodium Tetraphenylborate | HCID 2723787 | — |
| Product | HCID 15219578 | HCID 15219578 | 70% |
Reaction Steps
14.9 g (0.1 mol) of 4-(N,N-dimethylamino)benzaldehyde were reacted with 23.6 g (0.1 mol) of 4-methyl-N-methylpyridinium iodide, prepared according to Example 3, and the resulting solution was treated with 34.6 g (0.1 mol) of sodium tetraphenyborate, under the conditions described in Example 6, to form dye2 as a red solid in a yield of 70%. 1H-NMR (DMSO-d6) δ 3.00 (s, 6H), 4.1 (s, 3H), 6.70 (t, 4H), 6.8 (t, d, 2H), 6.9 (t, 8H), 7.02 (d, 1H), 7.10 (d, 8H) 7.50 d, 2H), 7.9 (d, 2H), 8.62 (d, 2H) ppm. Td 266° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06402037B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-9787b74aace64ec5bdafd3de599b5f2b |
| Source note | uspto-grants-2002_06 |