HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1498007Generated: October 31, 2026
Bromine → 2-bromo-1-[1-methyl-5-(4-methylphenyl)-1H-pyrazol-4-yl]ethanone
https://huagongshe.com/reaction/1498007
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-[1-methyl-5-(4-methylphenyl)-1H-pyrazol-4-yl]ethanone | HCID 68182054 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-bromo-1-[1-methyl-5-(4-methylphenyl)-1H-pyrazol-4-yl]ethanone | HCID 86669716 | — |
Reaction Steps
Bromine (97%, 0.104 mL, 1.97 mmol) was added to a solution of 1-[1-methyl-5-(4-methylphenyl)-1H-pyrazol-4-yl]ethanone (420 mg, 1.96 mmol) in glacial acetic acid (10 mL), and the reaction mixture was vigorously stirred for 2 hours at 80° C. After removal of solvent under reduced pressure, the residue was diluted with ethyl acetate, washed with saturated aqueous sodium bicarbonate solution, washed with saturated sodium chloride solution and dried over sodium sulfate. Filtration and concentration of the filtrate in vacuo provided a residue, which was purified via silica gel chromatography (Gradient: 10% to 30% ethyl acetate in heptane) to afford the product as a colorless oil. Yield: 353 mg, 1.20 mmol, 61%. LCMS m/z 293.1 (M+1). 1H NMR (400 MHz, CDCl3) δ 2.46 (s, 3H), 3.71 (s, 3H), 3.97 (s, 2H), 7.31 (br AB quartet, JAB=8 Hz, ΔvAB=23 Hz, 4H), 8.05 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09200000B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-eb37771702f049b693ed30f0f7bd80a0 |
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| Source note | uspto-grants-2015_12 |
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