HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → 4-Chloro-N-hydroxybenzimidoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | (NZ)-N-[(4-chlorophenyl)methylidene]hydroxylamine;4-fluorobenzaldehyde | HCID 87630081 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloro-N-hydroxybenzimidoyl chloride | HCID 7271865 | 86.4% |
Reaction Steps
To a solution of (E)- and/or (Z)-4-chloro-benzaldehyde oxime 4-fluorobenzaldehyde (27.0 g, 173 mmol) in DMF (173 mL) was added N-chlorosuccinimide (22.8 g, 173 mmol) portionwise over 1 h, keeping the temperature below 35° C. The reaction mixture was stirred at room temperature for 1 h. 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 sulfate and evaporated to afford the title compound (28.4 g, 86%) which was obtained as a light yellow solid. MS: m/e=189.1 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604062B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-89e21046a7b846fd8e5313bbbe87caa2 |
| Source note | uspto-grants-2013_12 |