HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Benzyl-4,5-dichloro-2,3-dihydropyridazin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178518919 | HCID 178518919 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Benzyl-4,5-dichloro-2,3-dihydropyridazin-3-one | HCID 722438 | 96.4% |
Reaction Steps
To a stirring suspension of 4,5-dichloro-3-hydroxypyridazine (33 g, 200 mmol) in DMF (260 mL) at room temperature under argon was added K2CO3 (55 g, 400 mmol), followed by benzyl bromide (41 g, 505.8 mmol). After 16 h the reaction mixture was poured into a flask containing water (500 mL) with stirring. After 15 min stirring, the precipitated product was collected by filtration and washed thoroughly with water. The solid was dried in a vacuum oven at 50° C. for 16 h to obtain the title compound, 2-benzyl-4,5-dichloropyridazin-3(2H)-one, (49.2 g, 96%) as an off-white solid. MS [M+H]+ 255; HPLC retention time=3.02 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07378418B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-a785c87a78b743f0ae004f0277332b45 |
| Source note | uspto-grants-2008_05 |