HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → Alpha-chlorobenzaldoxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Syn-benzaldehyde oxime | HCID 5324470 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Alpha-chlorobenzaldoxime | HCID 5706359 | 87% |
Reaction Steps
To a solution of (E)- and/or (Z)-benzaldehyde-oxime (5.27 g, 44 mmol) in DMF (44 mL) was added N-chlorosuccinimide (5.81 g, 44 mmol) portionwise over 1 h, keeping the temperature below 35° C. The reaction mixture was stirred at room temperature overnight. The mixture was then poured onto ice-water, and extracted with ethyl acetate. The combined organic layers were then washed with water and brine, dried over sodium sulphate and evaporated to afford the title compound (5.91 g, 87%) which was obtained as a light yellow solid. MS m/e (EI): 155.0 [M].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414061B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-d7ffc38c69cb4108bb7f9423e7f8b582 |
| Source note | uspto-grants-2008_08 |