HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzaldehyde → N-(4-Methoxybenzylidene)-N-(4-methoxybenzyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Product | N-(4-Methoxybenzylidene)-N-(4-methoxybenzyl)amine | HCID 578709 | 131% |
Reaction Steps
4-Methoxybenzylamine (40 g, 290 mmol) was cooled to 0° C., and p-anisaldehyde (39.7 g, 292 mmol) was added dropwise. The reaction was stirred at ambient temperature for two hours, concentrated under reduced pressure, and further dried under high vacuum overnight to provide 97 g of N-(4-methoxybenzyl)-N-[(4-methoxyphenyl)methylidene]amine as a white, waxy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143270B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-b566f8d0d4604980b48691a32407a87c |
| Source note | uspto-grants-2012_03 |