HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Dimethoxybenzaldehyde → 2-[(2,5-Dimethoxybenzylidene)amino]-3-methylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Dimethoxybenzaldehyde | HCID 66726 | — |
| Reactant | 2-[(5-Methoxy-2-methoxymethoxybenzylidene)amino]-3-methylphenol | HCID 21959323 | — |
| Product | 2-[(2,5-Dimethoxybenzylidene)amino]-3-methylphenol | HCID 21959334 | — |
Reaction Steps
2-[(2,5-dimethoxybenzylidene)amino]-3-methylphenol (F7) was prepared in a similar manner for the preparation of 2-[(5-Methoxy-2-methoxymethoxybenzylidene)amino]-3-methylphenol (F4) by using 2,5-dimethoxybenzaldehyde (3.32 g, 20 mmol) instead of 5-methoxy-2-methoxymethoxybenzaldehyde (F1) in 82% (4.44 g): 1H-NMR (400 MHz, CDCl3) δ2.32 (s, 3H), 3.84 (s, 6H), 6.77 (d, 1H, J=7.6 Hz), 6.82 (d, 1H, J=2.0 Hz), 6.83 (d, 1H, J=7.6 Hz), 6.91 (d, 1H, J=9.2 Hz), 6.99 (t, 1H, J=7.6 Hz), 7.06 (dd 1H, J=9.2, 2.0 Hz), 7.69 (s, 1H), 8.94 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105680B1 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-a5bd40493ca54e359f3b56ed6a06bfa6 |
| Source note | uspto-grants-2006_09 |