HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 86586364, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | N-tert-butylhydroxylamine | HCID 98586 | — |
| Reactant | HCID 15550539 | HCID 15550539 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 86586364 | HCID 86586364 | 56.5% |
Reaction Steps
To a solution of 4-pentanoyl-3,5-di-tert-butylbenzaldehyde (17.48 g, 0.050 mol) in benzene (250 mL) was added tert-butylhydroxylamine (4.57 g, 0.0510 mol) and p-toluenesulfonic acid (0.080 g). Using a Dean-Stark trap, the resulting mixture was refluxed until no more aldehyde was detected by TLC (Rf=0.43 for product using 1:1 hexanes/EtOAc). The solvent was removed in vacuo and the residue was thoroughly washed with hexanes. The title compound was isolated (56.50% yield) as a white solid, m.p. 195.5–204.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06998419B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-73ccb4de09c54d1cb1ec8c18acc0577b |
| Source note | uspto-grants-2006_02 |