HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244945Generated: October 30, 2026
Acetone cardice → HCID 178440337, compound
https://huagongshe.com/reaction/244945
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone cardice | HCID 18522661 | — |
| Reactant | HCID 67815312 | HCID 67815312 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178440337 | HCID 178440337 | — |
Reaction Steps
1.60 g (3.63 mmol) of 4-bromo-3-isopropyl-1-(2-methyl-1-phenylpropan-2-yl)-1H-pyrazol-5-yl benzoate was dissolved in 16 mL of tetrahydrofuran and cooled with a coolant (acetone/dry ice) to −60° C., and after dropwise addition of 2.60 ml (4.24 mmol) of 1.63 M n-butyllithium in n-hexane, stirred at 72° C. for 4 hours under a nitrogen atmoephere. The reaction was quenched with distilled water, and the reaction solution was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (silica gel12 g, ethyl acetate:hexane=1:20) to give 520 mg of the desired product as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658686B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-1bc68b47b376400b9b6eddc7cbb0389e |
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| Source note | uspto-grants-2014_02 |
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