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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | 1-(3-Phenylbenzo[b]thiophen-2-yl)ethanol | HCID 58459157 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(1-Azidoethyl)-3-phenylbenzo[b]thiophene | HCID 86668869 | 55.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653089B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-6f4102964e4847998231a8d733a70dc7 |
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| Source note | uspto-grants-2014_02 |
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