HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → 4-t-Butoxycarbonyl benzaldoxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tert-butyl 4-cyanobenzoate | HCID 271408 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-t-Butoxycarbonyl benzaldoxime | HCID 86753787 | 51.3% |
Reaction Steps
In 100 ml of methanol were dissolved 20.5 g of 4-cyanobenzoic acid t-butyl ester and 13.9 g of hydroxylamine. To the solution was added, while stirring at room temperature, 128 g of triethylamine, and the mixture was stirred for one hour at 85° C. The reaction mixture was concentrated under reduced pressure. The concentrate was dissolved in ethyl acetate, and the solution was washed with water. The organic layer was concentrated under reduced pressure to give a crude product, which was recrystallized from isopropyl ether to afford 11.45 g of the title compound as a colorless crystalline product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06020334 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-04dbb81ec03d48a5af32ad171d108224 |
| Source note | uspto-grants-2000_02 |