HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750971Generated: October 26, 2026
Triphenylphosphine → 4-(4-[1,2,3]Triazol-1-yl-but-1-enyl)-phenol
https://huagongshe.com/reaction/750971
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-4-iodobenzene | HCID 14803527 | — |
| Reactant | 1-but-3-enyl-1H-[1,2,3]triazole | HCID 19068208 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-(4-[1,2,3]Triazol-1-yl-but-1-enyl)-phenol | HCID 69291800 | — |
Reaction Steps
A mixture of 3.00 g (24.4 mmol) 1-but-3-enyl-1H-[1,2,3]triazole, 6.79 g (20.3 mmol) tert-butyl-(4-iodo-phenoxy)-dimethyl-silane, 1.07 g (4.06 mmol) triphenylphosphine, 0.685 g (3.05 mmol) palladium(II)acetate and 56 ml triethylamine was heated to reflux for 24 h. The reaction mixture was cooled to r.t., evaporated, stirred with ice and adjusted to pH=1 by addition of conc. HCl. The organic material was collected with ethyl acetate/dichloromethane 1:2, the organic phase dried over sodium sulfate and evaporated. The residue was stirred with 20.3 ml 1M solution of tetrabutylammonium fluoride solution in THF at 28° C. for 3 h. After removal of THF, the residue was dissolved in dichloromethane, washed with water, evaporated and purified by chromatography on silica gel (ethyl acetate/n-heptane 5:1). The product containing fractions were collected, evaporated and stirred with little ethyl acetate/n-heptane 3:1 to yield 1.53 g (29%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405231B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-0eb27830ab684523ad1a5a413a2c58ed |
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| Source note | uspto-grants-2008_07 |
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