HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloral alcoholate → N-(2-chloro-4-fluorophenyl)-2-(N-hydroxyimino)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloral alcoholate | HCID 10587 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Benzenamine, 2-chloro-4-fluoro- | HCID 75013 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-chloro-4-fluorophenyl)-2-(N-hydroxyimino)acetamide | HCID 22612791 | 3,437% |
Reaction Steps
A solution containing NH2OH.HCl (3.2 g, 46 mmol), anhydrous sodium sulphate (13 g, 93 mmol), and 2.2.2-trichloro-1-ethoxy ethanol (4.1 g, 21.2 mmol) in water (60 mL) was added to a solution of 2-chloro-4-fluroaniline (2 g, 0.27 mmol) in 4 M HCl (25 mL). The solution was refluxed for 40 minutes forming a white precipitate in the process. The mixture was cooled to room temperature, extracted with ethyl acetate three times, dried over sodium sulfate, filtered and concentrated in vacuo to provide 2.01 g of N-(2-chloro-4-fluoro-phenyl)-2-((E)-hydroxyimino)-acetamide: 1H NMR (300 MHz, CDCl3) δ 8.8 (bs, 1H), 8.4 (dd, 1H), 7.9 (s, 1H), 7.6 (s, 1H), 7.2 (dd, 1H), 7.0 (ddd, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552186B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-aa1631e8f3684d9dae27d31f1d491861 |
| Source note | uspto-grants-2013_10 |