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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179400Generated: October 26, 2026

Sodium Azide → 2-(2-Azidoethyl)-5-bromo-7-chlorobenzofuran

https://huagongshe.com/reaction/2179400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant2-(5-Bromo-7-chlorobenzofuran-2-yl)ethyl 4-methylbenzenesulfonateHCID 86668003—
SolventDimethylformamideHCID 6228—
Product2-(2-Azidoethyl)-5-bromo-7-chlorobenzofuranHCID 8666800475%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of the product of step C (2.3 g, 5.35 mmol) in dimethylformamide (11 mL) was added sodium azide (1.2 g, 18.73 mmol) at ambient temperature. The reaction mixture was heated at 70° C. for 2 h, cooled and quenched with water then extracted with ethyl acetate (2×15 mL). The combined organic extracts were dried over Na2SO4 and concentrated in vacuo to give the crude product which was purified by column chromatography (SiO2, 4:1 hexanes/ethyl acetate) providing 2-(2-azidoethyl)-5-bromo-7-chlorobenzofuran (1.2 g, 75%) as an off-white solid: 1H NMR (CDCl3, 400 MHz) δ 7.52-7.49 (m, 1H), 7.37-7.35 (m, 1H), 6.50 (s, 1H), 3.67 (t, J=6.8 Hz, 2H), 3.07 (t, J=6.8 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067949B2
Source datasetuspto-grants-2015_06
ORD IDord-f7b1bc037543499a923c143918cd1abf
Source noteuspto-grants-2015_06