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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075138Generated: October 25, 2026

Benzofuran, 5-bromo- → 5-Isobutylbenzofuran

https://huagongshe.com/reaction/2075138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzofuran, 5-bromo-HCID 90015—
ReactantHCID 178448254HCID 178448254—
CatalystHCID 178418851HCID 178418851—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-IsobutylbenzofuranHCID 2340363474.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

5-bromobenzofuran (500 mg, 2.56 mmol) was dissolved in THF solution of isobutylzinc(II) bromide (0.5M, 15 mL, 7.40 mmol) in a microwave reaction tube. Pd(PtBu3)2 (65 mg, 0.128 mmol, 0.05 eqv.) was added to this solution. The mixture was purged with N2 gas for 3-5 min and heated at 100° C. for 30 min under microwave irradiation. Upon completion of the reaction, the reaction mixture was diluted with ethyl acetate, washed with 1N HCl aqueous solution, brine, filtered through Celite. The filtrate was dried over Na2SO4 and concentrated. The residue was purified by silica gel column chromatography (ISCO system, 5% EtOAc in hexanes) to give 0.331 g desired product (74% yield): 1H NMR (400 MHz, CDCl3) δ 7.59 (s, 1H), 7.35 (d, 1H), 7.07 (d, 1H), 6.70 (s, 1H), 2.59 (d, 2H), 1.9 (m, 1H), 0.9 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919519B2
Source datasetuspto-grants-2011_04
ORD IDord-9f61e3591a404270ab4b0b3749aa2342
Source noteuspto-grants-2011_04