HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926745Generated: October 31, 2026
Tetrabutylammonium Fluoride → HCID 57743036, compound
https://huagongshe.com/reaction/1926745
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 53629161 | HCID 53629161 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57743036 | HCID 57743036 | 14% |
Reaction Steps
In a 100 ml flask fitted with a magnetic stirrer and a reflux condenser under inert atmosphere, 1-({3,5-dimethyl-1-[(4-methylphenyl)sulfonyl]-1H-pyrazol-4-yl}methyl)-4-(2,3,5-trifluorophenyl)pyrrolidin-2-one x61 (0.83 g, 1.7 mmol) is dissolved in THF (40 ml). A 1 M solution of tetrabutylammonium fluoride in THF (1.7 ml, 1.7 mmol) is added and the mixture is heated at 85° C. for 48 h. The solvent is evaporated and the residue is dissolved in water. The aqueous phase is extracted six times with diethylether and the combined organic phases are dried over MgSO4, filtered and concentrated in vacuo. The crude product is purified by preparative chromatography on silicagel and recrystallized from AcOEt to give 77 mg of 1-[(3,5-dimethyl-1H-pyrazol-4-yl)methyl]-4-(2,3,5-trifluorophenyl)pyrrolidin-2-one 167.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183241B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-2382608770d6492f93a84bfa71e94fb9 |
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| Source note | uspto-grants-2012_05 |
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