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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454801Generated: October 30, 2026

1-Iodo-4-nitrobenzene → 2-(4-Nitrophenyl)-4-methoxybenzothiophene

https://huagongshe.com/reaction/454801

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Iodo-4-nitrobenzeneHCID 12495—
Reactant(4-Methoxybenzo[b]thiophen-2-yl)boronic acidHCID 21182781—
CatalystSodium CarbonateHCID 10340—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(4-Nitrophenyl)-4-methoxybenzothiopheneHCID 4694696191.3%

Reaction Steps

To a suspension of anhydrous 1,2-dimethoxyethane (DME, 20 mL) containing a palladium tetrakis catalyst (Pd(PPh3)4 (49.7 mg, 0.043 mmol) was added 4-iodonitrobenzene (535.8 mg, 2.15 mmol), stirred at room temperature for 10 minutes, followed by adding 4-methoxybenzothiophene-2-boronic acid (95a, 470 mg, 2.26 mmol) and 2.0 M sodium carbonate aqueous solution (43 mL, 0.086 mmol). The reaction mixture was heated to reflux for 10 hours and cooled to room temperature, and ice water was added. The resulting product was extracted with ethyl acetate, evaporated after a treatment with, and purified by column chromatograph to give the target compound 2-(4-nitrophenyl)-4-methoxybenzothiophene (1-1, 560 mg, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497260B2
Source datasetuspto-grants-2013_07
ORD IDord-65192d248a6141eeae3e1a305b2f7d85
Source noteuspto-grants-2013_07