HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 4-bromo-1-butyl-5-methyl-1H-pyrazole-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 1-butyl-5-methyl-1H-pyrazole-3-carbonitrile | HCID 66958617 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-bromo-1-butyl-5-methyl-1H-pyrazole-3-carbonitrile | HCID 66958622 | 101.1% |
Reaction Steps
1-Butyl-5-methyl-1H-pyrazole-3-carbonitrile (6.58 g, 38 mmol) was treated with potassium acetate (57.2 mmol) and bromine (41.9 mmol) in acetic acid (50 mL) according to a modification of the method described in Part F of Examples 1-4. The reaction provided 9.3 g of 4-bromo-1-butyl-5-methyl-1H-pyrazole-3-carbonitrile as a colorless oil that crystallized upon standing. The crystals were used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879849B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-db890ab5649345a9945db642a127ffdf |
| Source note | uspto-grants-2011_02 |