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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243128Generated: November 2, 2026

Triphenylphosphine → HCID 86600004, compound

https://huagongshe.com/reaction/2243128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 68593443HCID 68593443—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86600004HCID 8660000480%

Reaction Steps

To 2-ethyl-1-[1-(4-methoxyphenyl)-1H-pyrazol-5-yl]butan-1-ol (1.0 g, 3.7 mmol) in THF (35 mL) at 0° C. was added triphenylphosphine (1.5 g, 5.6 mmol), diethyl azodicarboxylate (0.88 mL, 5.6 mmol) and diphenylphosphorylazide (1.2 mL, 5.6 mmol). The reaction mixture was slowly warmed to room temperature and stirred for 18 h. The reaction mixture was diluted with EtOAc and washed twice with 1N HCl. The organic layer was dried (MgSO4), filtered, concentrated in vacuo and the resulting oil was purified by column chromatography (SiO2, EtOAc/hexane, 1:9) to give a clear oil in 80% yield. 1H NMR (400 MHz, DMSO-d6) δ 7.66 (d, 1H, J=1.9 Hz), 7.32 (m, 2H), 7.07 (m, 2H), 6.55 (m, 1H), 4.42 (d, 1H, J=8.4 Hz), 3.80 (s, 3H), 1.60 (m, 1H), 1.41 (m, 1H), 1.25 (m, 1H), 1.14 (m, 2H), 0.69 (t, 3H, J=7.4 Hz), 0.60 (t, 3H, J=7.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674813B2
Source datasetuspto-grants-2010_03
ORD IDord-c43681484de14402b7e504a55d77d5cd
Source noteuspto-grants-2010_03