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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Fluoro-3-iodobenzene | HCID 70725 | — |
| Reactant | 1-Benzothiophene-3-carbaldehyde | HCID 227328 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Catalyst | Tris(furan-2-yl)phosphane | HCID 521585 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 89760791 | HCID 89760791 | 76.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334292B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-5cde419c9a544f88a8a8b7072edd660f |
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| Source note | uspto-grants-2016_05 |
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