HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-tert-butylhydroxylamine → HCID 86587913, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-tert-butylhydroxylamine | HCID 98586 | — |
| Reactant | 4-[(4-Fluorophenyl)methoxy]benzaldehyde | HCID 735860 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 86587913 | HCID 86587913 | — |
Reaction Steps
The title compound was prepared by refluxing a benzene solution of 4-(4-fluorobenzyloxy)benzaldehyde and N-tert-butylhydroxylamine for 21 hours with p-toluenesulfonic acid as a catalyst. The title compound was obtained as a solid in 98.5% yield, m.p. 180.3° C. (Rf =0.16 on a silica gel plate using hexanes: EtOAc, 1:1, v/v, as an eluant).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046232 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-2d0a2704762743e5aa68666eb89ed91b |
| Source note | uspto-grants-2000_04 |