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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071067Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-(Azidomethyl)benzofuran

https://huagongshe.com/reaction/2071067

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant1-Benzofuran-2-YlmethanolHCID 2776263—
SolventTolueneHCID 1140—
Product2-(Azidomethyl)benzofuranHCID 86647433—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of 1.00 g (6.77 mmol) of benzofuran-2-ylmethanol in 10 mL of toluene at r.t. was added 1.7 mL (7.89 mmol) of DPPA. The solution was cooled to 0° C. and 1.2 ml (8.02 mmol) of DBU was added. The ice bath was removed, and the mixture was stirred with warming to r.t. After 12.5 h, 1N HCl was added to a pH=4, and the aqueous layer was extracted with EtOAc. The pH of the aqueous layer was then adjusted to pH=6 with saturated NaHCO3 solution, and the aqueous layer was extracted with EtOAc. The combined extracts were washed with brine, dried over Na2SO4, filtered, and concentrated. Purification by flash silica gel chromatography (5% EtOAc/hexanes) provided 2-(azidomethyl)benzofuran as a pale yellow oil in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-dbfe35826e9c49a99bc89500510c3095
Source noteuspto-grants-2012_10