HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 2-(4,5-Dibromo-6-oxopyridazin-1(6H)-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-(4,5-dibromo-6-oxopyridazin-1(6H)-yl)acetate | HCID 59574424 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(4,5-Dibromo-6-oxopyridazin-1(6H)-yl)acetic acid | HCID 59574142 | 96% |
Reaction Steps
Ethyl 2-(4,5-dibromo-6-oxopyridazin-1(6H)-yl)acetate (6.01 g, 17.7 mmol) in 1,4-dioxane (60 mL) was stirred with 1 M aqueous sodium hydroxide (53.1 mL, 53.1 mmol) at room temperature for 1 hour. After completion of the reaction, the reaction solution was mixed with ethyl acetate and extracted with 1 M aqueous sodium hydroxide twice. The resulting aqueous layer was acidified to pH 1 with 1 M hydrochloric acid and extracted with ethyl acetate twice. The resulting organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated under reduced pressure to give the desired product (5.30 g, 88% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08440666B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-0c764b9f1b244dc291c5f81eaed21270 |
| Source note | uspto-grants-2013_05 |