HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560565Generated: October 31, 2026
Triphenylphosphine → 2-(Azidomethyl)-5-(difluoromethyl)furan
https://huagongshe.com/reaction/560565
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | (5-(Difluoromethyl)furan-2-yl)methanol | HCID 20079677 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Azidomethyl)-5-(difluoromethyl)furan | HCID 86645289 | 77% |
Reaction Steps
To a solution of (5-(difluoromethyl)furan-2-yl)methanol (0.55 g, 3.72 mmol), triphenylphosphine (1.07 g, 4.09 mmol) and diethylazodicarboxylate (0.64 mL, 4.09 mmol) in anhydrous tetrahydrofuran (20 mL) was added diphenylphosphorylazide (0.88 mL, 4.09 mmol). The reaction mixture was stirred at ambient temperature for 18 hours, diluted with dichloromethane (40 mL) and washed with water and brine. The organic solution was dried over anhydrous sodium sulphate, filtered and concentrated in vacuo. The residue was purified by column chromatography eluted with ethyl acetate/hexane (1/9) to afford 2-(azidomethyl)-5-(difluoromethyl)furan as a yellow oil in 77% yield (0.50 g): 1H NMR (300 MHz, CDCl3) δ 6.61 (d, J=3.3 Hz, 1H), 6.58 (t, J=54.3 Hz, 1H), 6.37 (d, J=3.3 Hz, 1H), 4.30 (s, 2H); MS (ES+) m/z 172.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08063084B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-1943ff4e88df4bb5bf7c745eea596efb |
|---|
| Source note | uspto-grants-2011_11 |
|---|