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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050967Generated: November 2, 2026

Water → HCID 89525383, compound

https://huagongshe.com/reaction/1050967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 89525540HCID 89525540—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 89525383HCID 8952538337%

Reaction Conditions

Temperature0 °C

Reaction Steps

8.77 g (31.8 mmol, 1.2 eq) of diphenylphosphoryl azide were added dropwise to a solution of 5.21 g (26.5 mmol, 1 eq) of (5-methylfuran-2-yl)-(2-methyltetrahydrofuran-2-yl)methanol in 90 ml of toluene. The reaction medium was cooled to 0° C. and then 4.75 ml (31.8 mmol, 1.2 eq) of 1,8-diazabicyclo[5.4.0]undec-7-ene were added dropwise. The reaction medium was stirred at ambient temperature for 41 hours. The (heterogeneous) reaction medium was treated with water and with ethyl acetate and then separated by settling out. The organic phase was washed with 1 N hydrochloric acid, dried over magnesium sulfate, filtered and evaporated. The residue was chromatographed on HP silica gel (column puriFlash IR50SI-200G, Spot II) eluted with heptane/ethyl acetate (95/5). 2.15 g of 2-[azido-(2-methyltetrahydrofuran-2-yl)methyl]-5-methylfuran were obtained. Yield=37%. TLC/SiO2: heptane/EtOAc (80/20), developing with KMnO4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388149B2
Source datasetuspto-grants-2016_07
ORD IDord-d34e0fa97c834683829c3b6ea952f3b9
Source noteuspto-grants-2016_07