HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 86586362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | N-tert-butylhydroxylamine | HCID 98586 | — |
| Reactant | HCID 15550534 | HCID 15550534 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 86586362 | HCID 86586362 | 50.2% |
Reaction Steps
To a solution of 4-n-butanoyl-3,5-di-tert-butylbenzaldehyde (9.63 g, 0.032 mol) in benzene (200 mL) was added tert-butylhydroxylamine (3.52 g, 0.040 mol) and p-toluenesulfonic acid (0.100 g). Using a Dean-Stark trap, the resulting solution was refluxed until no more aldehyde was detected by TLC (Rf=0.30 for product and 0.91 for starting material using 3:1 hexanes/EtOAc). The solvent was removed in vacuo and the residue was crystallized from EtOAc and hexanes to afford the titled compound (50.2% yield) as a white solid, m.p. 216.9–236.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06998419B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-34ceb3f4b1934ae89f0f667eb4804bbc |
| Source note | uspto-grants-2006_02 |