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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067338Generated: November 1, 2026

Triphenylphosphine → 2-(Azidomethyl)-5-(difluoromethyl)furan

https://huagongshe.com/reaction/2067338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant(5-(Difluoromethyl)furan-2-yl)methanolHCID 20079677—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-(Azidomethyl)-5-(difluoromethyl)furanHCID 8664528977%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293768B2
Source datasetuspto-grants-2012_10
ORD IDord-cff9a5fea9b342778c8633fd23e4199c
Source noteuspto-grants-2012_10