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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64129Generated: October 26, 2026

Nitrogen → N-(3-(benzofuran-2-yl)-5-nitrophenyl)acetamide

https://huagongshe.com/reaction/64129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSodium CarbonateHCID 10340—
ReactantN-(3-bromo-5-nitrophenyl)acetamideHCID 10658908—
Reactant2-(1-Benzofuran-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 11368533—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductN-(3-(benzofuran-2-yl)-5-nitrophenyl)acetamideHCID 89500178—

Reaction Steps

A solution of N-(3-bromo-5-nitrophenyl)acetamide of Example 1(c) (2 g, 7.7 mmol) in 1,2-dimethoxyethane (25 ml) was degassed by N2 bubbling for 5 min. 2-(Benzofuran-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.45 g, 10 mmol, 1.3 eq.) was added and the mixture was degassed for another 5 min. Pd(dppf)Cl2 (0.63 g, 0.77 mmol, 0.1 eq.) and aqueous sodium carbonate (2.45 g, 23.1 mmol, 3.0 eq.) were added and the procedure of Example 1(d) was followed. The crude residue of the product was directly used for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447091B2
Source datasetuspto-grants-2016_09
ORD IDord-1e27b309856a4d778203c36fa0fb4ba4
Source noteuspto-grants-2016_09