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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-4-iodobenzeneHCID 14803527—
Reactant1-but-3-enyl-1H-[1,2,3]triazoleHCID 19068208—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
Product4-(4-[1,2,3]Triazol-1-yl-but-1-enyl)-phenolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405231B2
Source datasetuspto-grants-2008_07
ORD IDord-0eb27830ab684523ad1a5a413a2c58ed
Source noteuspto-grants-2008_07