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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243151Generated: October 30, 2026

Triphenylphosphine → 5-(1-Azido-2-ethylbutyl)-1-(benzyloxy)-1H-pyrazole

https://huagongshe.com/reaction/2243151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant1-[1-(Benzyloxy)-1H-pyrazol-5-yl]-2-ethylbutan-1-olHCID 68593374—
SolventTetrahydrofuranHCID 8028—
Product5-(1-Azido-2-ethylbutyl)-1-(benzyloxy)-1H-pyrazoleHCID 8660000867.2%

Reaction Steps

To a stirred mixture of 1-[1-(benzyloxy)-1H-pyrazol-5-yl]-2-ethylbutan-1-ol (0.492 g, 1.79 mmol) in THF (17 mL) at 0° C. under a nitrogen atmosphere was added triphenyl phosphine (0.705 g, 2.69 mmol) followed by diethyl azodicarboxylate (0.42 mL, 2.7 mmol). Diphenyl phosphoryl azide (0.58 mL, 2.7 mmol) was then added over 4 min. The mixture was allowed to attain ambient temperature and stirred for 16 h. The solvent was then evaporated in vacuo producing a crude oil which was purified on a Biotage column (hexane/ethyl acetate, 9:1). This afforded the product as a clear colorless oil (0.36 g, 67%). Mass Spectrum (+ESI): 300 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674813B2
Source datasetuspto-grants-2010_03
ORD IDord-a0af0916fdc648c3a36330ab4ee21bbc
Source noteuspto-grants-2010_03