HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-formyl-N-benzyloxyamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | O-Benzylhydroxylamine | HCID 102313 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | N-formyl-N-benzyloxyamine | HCID 11423690 | 60% |
Reaction Steps
O-benzylhydroxylamine (4.63 g, 37 mmol) was dissolved into 89% formic acid (80 ml), and 30 ml of acetic anhydride was added dropwise thereto with keeping the temperature at 50 to 60° C. After adding acetic anhydride, the solution was stirred for 2 hours at room temperature. The organic layer was rinsed and dried, and the solvent was evaporated. The residue was then purified with silica gel chromatography to obtain 3.05 g of N-benzyloxyformamide (yield: 60%). The proton NMR spectrum of the compound is 4.82 bs, 4.93 bs (2H); 7.20-7.47 m (5H); 7.93 bs, 8.30 bs (1H) (solvent: CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919825 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-ff3d102ecad1414f8f96a3a6718aed52 |
| Source note | uspto-grants-1999_07 |