HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251536Generated: October 26, 2026
Isopropyltriphenylphosphonium bromide → HCID 69099725, compound
https://huagongshe.com/reaction/2251536
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyltriphenylphosphonium bromide | HCID 2795292 | — |
| Reactant | HCID 59643273 | HCID 59643273 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 69099725 | HCID 69099725 | 33.1% |
Reaction Steps
A solution of isopropyltriphenylphosphonium bromide (326 mg; 0.75 mmol) in 1.5 ml of dry THF was treated in an ice bath, under nitrogen, with n-butyl lithium (0.425 ml of a 1.6M solution in hexane; 0.68 mmol), dropwise. After stirring for 15 minutes, this mixture was added, via syringe, into an ice-cold solution of ethyl 2-[4-(2-{(5-formylpyridin-2-yl)[4-(trifluoromethoxy)benzyl]amino}ethyl)phenoxy]-2-methylpropanoate (200 mg; 0.38 mmol) in 2 ml of dry THF. After stirring at rt overnight, the reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed with water and brine, dried over sodium sulfate, filtered and concentrated. Purification by radial chromatography using ethyl acetate-hexane mixtures (5–20% gradient) afforded ethyl 2-methyl-2-[4-(2-{[5-(2-methylprop-1-enyl)pyridin-2-yl][4-(trifluoromethoxy)benzyl]amino}ethyl)phenoxy]propanoate (70 mg; 33% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07319104B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-f08de614410e444ba5cbf1e46474f706 |
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| Source note | uspto-grants-2008_01 |
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