HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetic Acid → 2-(4-nitro-1H-pyrazol-1-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetic Acid | HCID 6227 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-nitro-1H-pyrazole | HCID 16376 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-nitro-1H-pyrazol-1-yl)acetic acid | HCID 1283477 | 88% |
Reaction Steps
A solution of potassium hydroxide (32.7 g, 0.58 mol) in water (100 mL) was added to a stirred mixture of 4-nitro-1H-pyrazole (30 g, 0.27 mol) in acetone (500 mL) at room temperature. After 30 min, a solution of 2-bromoacetic acid (38.7 g, 0.27 mol) in acetone (100 mL) was added and the reaction was stirred overnight. The solvent was removed in vacuo, the residue was diluted with water then extracted three times with ethyl acetate and the combined organic layer was concentrated in vacuo. The residue was further extracted with dichloromethane and methanol and the combined organic layer was concentrated in vacuo to afford 2-(4-nitro-1H-pyrazol-1-yl)acetic acid (40 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296725B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-d236a53bbc18460e902edc237568ac13 |
| Source note | uspto-grants-2016_03 |