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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369114Generated: November 1, 2026

Benzofuran → HCID 18518550, compound

https://huagongshe.com/reaction/1369114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzofuranHCID 9223—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 10958318HCID 10958318—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18518550HCID 1851855021.2%

Reaction Steps

To benzo[b]furan (76.4 mg, 2.1 eq) in anhydrous THF (2 mL) at −40° C. (bath temperature) was added n-BuLi (0.423 mL, 1.53 M in hexanes, 2.1 eq). The resulting light yellow coloured solution was stirred for 30 minutes, after which 1-(2-diethylaminoethyl)-4-bromoisatin (100.0 mg, 3.08×10−4 mol) in anhydrous THF (2 mL) was added. Stirring was continued at −40° C. for 9 hours. Saturated aqueous NH4Cl (1.5 mL) was added and the mixture was allowed to warm to room temperature. The mixture was extracted with EtOAc and the combined extracts were dried (anhydrous Na2SO4). After filtration, the solvent was removed in vacuo. Purification was carried out by column chromatography (silica gel, eluting 1%-2% MeOH in CHCl3) to give the title compound as a yellow oil (29.0 mg, 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576656B1
Source datasetuspto-grants-2003_06
ORD IDord-8d91b6f526544b499b7203a9129bea33
Source noteuspto-grants-2003_06