HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,5-Dimethoxy-2-methoxymethoxybenzaldehyde → 2-[(4,5-Dimethoxy-2-methoxymethoxybenzylidene)amino]-3-methylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,5-Dimethoxy-2-methoxymethoxybenzaldehyde | HCID 21959322 | — |
| Reactant | 2-[(5-Methoxy-2-methoxymethoxybenzylidene)amino]-3-methylphenol | HCID 21959323 | — |
| Product | 2-[(4,5-Dimethoxy-2-methoxymethoxybenzylidene)amino]-3-methylphenol | HCID 21959313 | — |
Reaction Steps
2-[(4,5-dimethoxy-2-methoxymethoxybenzylidene)amino]-3-methylphenol (F5) was prepared in a similar manner for the preparation of 2-[(5-Methoxy-2-methoxymethoxybenzylidene)amino]-3-methylphenol (F4) by using 4,5-dimethoxy-2-methoxymethoxybenzaldehyde (F2) (2.26 g, 10 mmol) instead of 5-methoxy-2-methoxymethoxybenzaldehyde (F1) in 86% (2.80 g): 1H-NMR (500 MHz, CDCl3) δ3.53 (s, 3H), 5.24 (s, 3H), 7.17 (d, 1H, J=9.0 Hz), 7.35 (d, 1H, J=9.0 Hz), 10.52 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105680B1 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-568765deeac74bb3b38bd23ee461406a |
| Source note | uspto-grants-2006_09 |