HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → 2-Fluoro-N-hydroxybenzimidoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | (NZ)-N-[(2-fluorophenyl)methylidene]hydroxylamine | HCID 5372467 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Fluoro-N-hydroxybenzimidoyl chloride | HCID 9634577 | 250.9% |
Reaction Steps
To a solution of (E)- and/or (Z)-2-fluoro-benzaldehyde oxime (66.8 g, 480 mmol) in DMF (334 mL) was added N-chlorosuccinimide (29.4 g, 211 mmol) portionwise and after 10 min, keeping the temperature below 50° C., N-chlorosuccinimide (44.1 g, 317 mmol) was added portionwise. The reaction mixture was stirred at room temperature for 2 h and then extracted with tert-butyl methyl ether to afford the title compound (91.9 g, 91%) which was obtained as a yellow oil. 1H-NMR (CDCl3): 7.10-7.25 (m, 2H), 7.40-7.50 (m, 1H), 7.64-7.70 (m, 3H), 8.99 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846719B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-c1380732b0d1448fbc4dbf13122a5379 |
| Source note | uspto-grants-2014_09 |