HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244944Generated: October 30, 2026
Benzoyl chloride → HCID 67815312, compound
https://huagongshe.com/reaction/244944
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67811749 | HCID 67811749 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67815312 | HCID 67815312 | 85% |
Reaction Steps
4-Bromo-3-isopropyl-1-(2-methyl-1-phenylpropan-2-yl)-1H-pyrazol-5(4H)-one (3.00 g, 8.90 mmol) was dissolved in 39 mL of tetrahydrofuran and cooled with ice to 0° C., and after dropwise addition of 1.80 g (17.8 mmol) of triethylamine and 1.38 g (9.82 mmol) of benzoyl chloride, stirred at room temperature for 3 hours under a nitrogen atmosphere. The reaction was quenched with distilled water, and the reaction solution was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (silica gel 12 g, ethyl acetate:hexane=1:20) to give 3.34 g 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-3787d6a30bbf453fa0a6ba8df44c6adc |
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| Source note | uspto-grants-2014_02 |
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