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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271504Generated: October 30, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 4-[Azido-(5-methylfuran-2-yl)methyl]tetrahydropyran

https://huagongshe.com/reaction/2271504

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant(5-Methylfuran-2-yl)-(tetrahydropyran-4-yl)methanolHCID 63937679—
SolventTolueneHCID 1140—
Product4-[Azido-(5-methylfuran-2-yl)methyl]tetrahydropyranHCID 8952543570%

Reaction Conditions

Temperature0 °C

Reaction Steps

6.08 g (22 mmol, 1.1 eq) of diphenylphosphoryl azide were added dropwise to a solution of 4.43 g (20 mmol, 1 eq) of (5-methylfuran-2-yl)-(tetrahydropyran-4-yl)methanol at 89% in 60 ml of toluene. The reaction medium was cooled to 0° C. and then 3.3 ml (22 mmol, 1.1 eq) of 1,8-diazabicyclo[5.4.0]undec-7-ene were added dropwise. The reaction medium was stirred at ambient temperature for 22 hours. The reaction medium was separated by settling out and the organic phase was washed with water and then with 1 N hydrochloric acid, dried over magnesium sulfate, filtered and evaporated. The residue was chromatographed on silica gel (column Analogix SF40-240 g, Spot II) eluted with heptane/ethyl acetate (95/5). 3.09 g of 4-[azido-(5-methylfuran-2-yl)methyl]tetrahydropyran were obtained. Yield=70%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120772B2
Source datasetuspto-grants-2015_09
ORD IDord-fb9881ffad204637ac2b5dff242c6948
Source noteuspto-grants-2015_09