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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242881Generated: October 31, 2026

Triphenylphosphine → 2-(1-Azidoethyl)-3-phenylbenzo[b]thiophene

https://huagongshe.com/reaction/242881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant1-(3-Phenylbenzo[b]thiophen-2-yl)ethanolHCID 58459157—
Solvent1,4-DioxaneHCID 31275—
Product2-(1-Azidoethyl)-3-phenylbenzo[b]thiopheneHCID 8666886955.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

DIAD (556 mg, 2.75 mmol) was added to a solution of triphenylphosphine (722 mg, 2.75 mmol) in dioxane (5 mL) at 0° C. under a nitrogen atmosphere. After 10 min, 1-(3-phenylbenzo[b]thiophen-2-yl)ethanol (350 mg, 1.37 mmol) was added followed by diphenylphosphoryl azide (454 mg, 1.65 mmol). The reaction mixture was stirred 20° C. for 16 h then concentrated in vacuo. The crude reaction mixture was purified by column chromatography (Si—PCC, gradient 0-20% DCM in cyclohexane) affording the title compound as a colourless oil (211 mg, 55%). 1H NMR (CDCl3, 400 MHz): δ 7.88 (1H, d, J=7.87 Hz), 7.54-7.42 (4H, m), 7.41-7.29 (4H, m), 4.97 (1H, q, J=6.80 Hz), 1.58 (3H, d, J=6.80 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-6f4102964e4847998231a8d733a70dc7
Source noteuspto-grants-2014_02