HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butylhydrazine monohydrochloride → 6-(4-Chlorophenyl)-4,5-dihydro-2-t-butylpyridazinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-Chlorobenzoylpropionic acid | HCID 18917115 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 6-(4-Chlorophenyl)-4,5-dihydro-2-t-butylpyridazinone | HCID 18917116 | 34.4% |
Reaction Steps
To a solution of 4-chlorobenzoylpropionic acid (4.24 g) in n-butanol (150 ml) was added anhydrous sodium acetate (1.54 g) and t-butylhydrazine hydrochloride (2.75 g) portionwise at room temperature. The resulting mixture was refluxed for 9 hours distilling off 65 ml of n-butanol during that time. The resulting mixture was cooled and poured into water (500 ml) and extracted with methylene chloride (3×150 ml). The combined organic layers were washed with 2% aqueous sodium hydroxide (3×100 ml), water (2×100 ml), 2% aqueous hydrochloric acid (3×100 ml), and water (1×100 ml), dried and evaporated under vacuum yielding 1.71 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05726176 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-d1cec5adaec74900a26ae5c2339bc4da |
| Source note | uspto-grants-1998_03 |