HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756949Generated: October 24, 2026
Triphenylundecylphosphonium bromide → HCID 54242059, compound
https://huagongshe.com/en/reaction/1756949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylundecylphosphonium bromide | HCID 3085198 | — |
| Reactant | ethyl (+/-)-4-formyl-alpha-phenyl-1H-pyrazole-l-acetate | HCID 10563150 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54242059 | HCID 54242059 | — |
Reaction Steps
A solution of n-BuLi (127 mL, 254 mmol, 2.0M in hexanes) was added dropwise to a suspension of n-undecyl-triphenylphosphonium bromide (121.6 g, 244 mmol, obtained from triphenylphosphine and undecylbromide) in 500 mL THF at -78° C. under an atmosphere of N2. The resulting orange solution was stirred for 1 hour before a solution of ethyl (±)-4-formyl-α-phenyl-1H-pyrazole-1-acetate in 250 mL THF was added dropwise. Warmed to room temperature and stirred for 16 hours. Quenched by adding 150 mL water and concentrating in vacuo. The residue was partitioned between water and dichloromethane. The organic layer was dried over MgSO4, filtered, and concentrated to give an oily tan solid. Triturated with boiling hexanes and filtered to remove triphenylphosphine oxide. The filtrate was concentrated and chromatographed (10% EtOAc/hexanes on silica) to give the title compound as a yellow oil, a 1:2 E/Z mixture (44.4 g, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05441975 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-c4de1ad2990442318a9ae27313a6992b |
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| Source note | uspto-grants-1995_08 |
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