HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(Chloromethyl)-N-hydroxybenzimidoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 4-Chloromethylbenzaldehyde oxime | HCID 76225737 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Chloromethyl)-N-hydroxybenzimidoyl chloride | HCID 76686601 | 113.9% |
Reaction Steps
4-(chloromethyl)benzaldehyde oxime 5 (15.8 g, 93.16 mmol) was dissolved in DMF (300 mL). NCS (13.69 g, 102.5 mmol) was added in portions and then HCl in dioxane (100 mL of 4 M, 400.0 mmol) was added slowly, cooling the mixture with an ice water bath to moderate the exotherm, keeping internal temperature below 33° C. The mixture was then stirred at room temperature for 1 hour. The solution was partitioned between EtOAc and water and the organic extract was washed with water and brine (5×200 ml), dried over MgSO4 and concentrated under reduced pressure to give a colourless solid (21.65 g, 95%). 1H NMR (400 MHz, CDCl3) δ 4.63 (2H, s), 7.45 (2H, d, J=8 Hz), 7.86 (2H, d, J=8 Hz), 8.36 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846686B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-20972544c6a147f59e18b4913de17036 |
| Source note | uspto-grants-2014_09 |