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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827486Generated: October 30, 2026

Triphenylphosphine → HCID 22136507, compound

https://huagongshe.com/reaction/1827486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAzideHCID 33558—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantSodium BicarbonateHCID 516892—
Reactant4-((Tert-butyldimethylsilyl)oxy)but-2-yn-1-olHCID 5461845—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22136507HCID 22136507—

Reaction Steps

To an ice cold, stirred solution of the known 4-(tert-Butyl-dimethyl-silanyloxy)-but-2-yn-1-ol (3.14 g, 15.7 mmol) in THF (50 ml) was added DBU (2.6 ml, 17.4 mmol) and DPPA (3.8 ml, 17.6 mmol). The solution was warmed to room temperature and stirred under an inert atmosphere overnight. The reaction was poured into sat. NaHCO3 and the layers separated. The aqueous layer was re-extracted with EtOAc (2×) and the combined organic layers were dried (Na2SO4), and concentrated under vacuum. Triphenylphosphine (4.61 g, 17.6 mmol) was added to this crude azide dissolved in THF (50 ml), followed by addition of H20 (0.44 ml). The resultant solution was stirred overnight at room temperature, concentrated under reduced pressure and the residue was slurried in a 1:1 mixture of Et2O/pet ether. The solids were removed and the filtrate was concentrated and purified by flash chromatography on silica gel eluting CH2Cl2/MeOH (19:1) to give an amber oil. 1H NMR (CDCl3) δ 4.19 (2H, t, J=1.9 Hz), 3.33 (2H, t, J=1.9 Hz), 0.79 (9H, s), 0.00 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053107B2
Source datasetuspto-grants-2006_05
ORD IDord-80594267981c498489dc24e21489af5b
Source noteuspto-grants-2006_05