HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 2-bromo-1-(1-methyl-1H-pyrazol-4-yl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(1-methyl-1H-pyrazol-4-yl)ethan-1-one | HCID 3596939 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-bromo-1-(1-methyl-1H-pyrazol-4-yl)ethan-1-one | HCID 43144152 | — |
Reaction Steps
To a solution of 1-(1-methyl-1H-pyrazol-4-yl)ethanone (0.602 g, 4.85 mmol) in chloroform (20 mL) and of 33% HBr in acetic acid (3.92 mg, 0.05 mmol) was added dropwise a chloroform solution containing Br2 (0.262 mL, 5.09 mmol) via an addition funnel. The reaction mixture was stirred at room temperature for 1 h and then concentrated under reduced pressure. The crude solid was triturated in ethyl acetate, filtered, washed and dried in vacuo. The free base was obtained by triturating the product in 5% NaHCO3 for 2 h. The solid that formed were collected by filtration, washed with water and isopropyl alcohol and then dried in vacuo. Isolation gave 874 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569484B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-620cd5c12e4643b6a007622b08c1974c |
| Source note | uspto-grants-2013_10 |