HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-hydroxybenzenecarboximidoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | (Z)-Benzaldehyde oxime | HCID 12143 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-hydroxybenzenecarboximidoyl chloride | HCID 2756315 | 89% |
Reaction Steps
To benzaldehyde oxime (12.2 g, 0.1 mol) in chloroform was added catalytic amount of pyridine, followed by N-chlorosuccinimide (13.35 g, 0.1 mol) at room temperature. The reaction mixture was stirred for 1.5 h, then saturated aqueous NaCl was added. The organic phase was washed with saturated aqueous NaCl (twice) and dried with MgSO4. The solvent was removed under reduced pressure. 13.85 g α-chlorobenzaldehyde oxime was obtained. The yield was 87%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07169798B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-e0e02c3fab8641aa9493a4ffcbcf26b0 |
| Source note | uspto-grants-2007_01 |