HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxy-2-methylbenzaldehyde → HCID 178458444, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxy-2-methylbenzaldehyde | HCID 458185 | — |
| Reactant | HCID 178458381 | HCID 178458381 | — |
| Product | HCID 178458444 | HCID 178458444 | — |
Reaction Steps
The title compound is prepared in analogy to 4-allyloxy-3-ethyl-N-hydroxy-5-methyl-benzamidine starting from commercially available 4-hydroxy-2-methyl-benzaldehyde; LC-MS: tR=0.62 min, [M+1]+=207.10; 13C NMR (CDCl3): δ 20.72, 68.91, 104.72, 112.75, 116.45, 118.32, 118.53, 132.25, 134.19, 144.09, 161.71.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08288554B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-32ee5df8d0d6401baaf54da2ccf3b8fa |
| Source note | uspto-grants-2012_10 |