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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523114Generated: October 31, 2026

1-Fluoro-3-iodobenzene → HCID 89760791, compound

https://huagongshe.com/reaction/523114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-3-iodobenzeneHCID 70725—
Reactant1-Benzothiophene-3-carbaldehydeHCID 227328—
ReactantMagnesium ChlorideHCID 5360315—
CatalystTris(furan-2-yl)phosphaneHCID 521585—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 89760791HCID 8976079176.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

A dry, argon-filled Schlenk tube with a magnetic stirrer bar and septum is initially charged with 1-benzothiophene-3-carbaldehyde (163 mg, 1 mmol) in anhydrous THF (1 ml). After adding (TMP)2Zn.MgCl2 (3.16 ml, 1.2 mmol) at 25° C., the mixture is stirred for 1 h, then a solution of 1-fluoro-3-iodobenzene (311 mg, 1.4 mmol), bis(dibenzylideneacetone)palladium(0) (17 mg, 3 mol %) and tri-2-furylphosphine (14 mg, 6 mol %) in anhydrous THF (2 ml) is added dropwise and the mixture is stirred at 25° C. overnight. For workup, the mixture is diluted with aqueous sat. NH4Cl solution (30 ml) and extracted with ethyl acetate (3×30 ml). After the combined organic phases have been dried over Na2SO4, the solvent has been distilled off and purification has been effected by column chromatography on silica gel (heptane:ethyl acetate), the desired compound (195 mg, 76% of theory) was obtained as a colourless crystalline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334292B2
Source datasetuspto-grants-2016_05
ORD IDord-5cde419c9a544f88a8a8b7072edd660f
Source noteuspto-grants-2016_05