HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397722Generated: November 1, 2026
Triphenylphosphine → HCID 57707801, compound
https://huagongshe.com/reaction/1397722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | (R)-1-(2-Chloro-8-fluoroquinolin-3-yl)ethanol | HCID 57707820 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57707801 | HCID 57707801 | — |
Reaction Steps
Triphenylphosphine (1.81 g, 6.9 mmol, 1.2 eq) was dissolved in anhydrous THF (30 mL) and cooled to 0° C. To this solution was added diispropylazodicarboxylate (1.36 mL, 6.9 mmol, 1.2 eq). The reaction was stirred for 30 minutes at 0° C. and (R)-1-(2-chloro-8-fluoroquinolin-3-yl)ethanol (1.3 g, 5.7 mmol) in 30 mL of THF was added, followed by diphenylphosphoryl azide (1.37 mL, 6.3 mmol, 1.1 eq). The reaction was allowed to warm to rt and stir at rt overnight. The reaction was deposited on silica gel and concentrated. Purification by column chromato-graphy (3% etoac in hexanes) afforded (S)-3-(1-azidoethyl)-2-chloro-8-fluoro-quinoline. 1H NMR (400 MHz, CDCl3) δ ppm 8.30 (d, J=1.2 Hz, 1H), 7.67 (br d, J=8.22 Hz, 1H), 7.54 (td, J=7.8, 4.7 Hz, 1H), 7.45 (ddd, J=10.2, 7.8, 1.2 Hz) 5.22 (q, J=6.7 Hz, 1H), 1.68 (d, J=6.7 Hz, 3H). Mass Spectrum (ESI) m/e=250.9 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08901135B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-5cb9560d8d7c4b3898d0642ed9795e75 |
|---|
| Source note | uspto-grants-2014_12 |
|---|