HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907175Generated: October 31, 2026
Lithium Chloride → 1-[1-methyl-5-(4-methylphenyl)-1H-pyrazol-4-yl]ethanone
https://huagongshe.com/reaction/1907175
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | 4-iodo-1-methyl-5-(4-methylphenyl)-1H-pyrazole | HCID 68182051 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[1-methyl-5-(4-methylphenyl)-1H-pyrazol-4-yl]ethanone | HCID 68182054 | — |
Reaction Steps
Tributyl(1-ethoxyvinyl)stannane (95%, 1.39 mL, 3.88 mmol) was added to a mixture of 4-iodo-1-methyl-5-(4-methylphenyl)-1H-pyrazole (768 mg, 2.58 mmol), tetrakis(triphenylphosphine)palladium(0) (298 mg, 0.258 mmol) and lithium chloride (98%, 279 mg, 6.45 mmol) in N,N-dimethylformamide (20 mL), and the reaction was stirred at 90° C. for 18 hours. After cooling, the mixture was filtered through Celite, and concentrated in vacuo; silica gel chromatography (Gradient: 10% to 50% ethyl acetate in heptane) afforded the product as a colorless oil. Yield: 460 mg, 2.15 mmol, 83%. LCMS m/z 215.3 (M+1). 1H NMR (400 MHz, CDCl3) δ 2.17 (s, 3H), 2.45 (br s, 3H), 3.69 (s, 3H), 7.28 (br AB quartet, JAB=8 Hz, ΔvAB=28 Hz, 4H), 7.99 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598155B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-fb00c166b9eb47cfa91b27744b8d26bb |
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| Source note | uspto-grants-2013_12 |
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