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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983872Generated: November 1, 2026

Hexane → 2-(2-nitrophenyl)thiophene

https://huagongshe.com/reaction/1983872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantPotassium CarbonateHCID 11430—
Reactanto-IodonitrobenzeneHCID 69115—
Reactant2-Thiopheneboronic acidHCID 2733960—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(2-nitrophenyl)thiopheneHCID 9167261107.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

14.07 g (110 mmol) of 2-thiophene-boronic acid, 24.9 g (100 mmol) of 1-iodo-2-nitrobenzene, and 5.78 g (5 mmol) of tetrakis(triphenylphosphine)palladium(0) were dissolved in 250 ml of ethylene glycol dimethyl ether (DME), and 70 ml of 2M K2CO3 aqueous solution was added to the solution, and then the mixture was refluxed at 80° C. for 12 hours. After the reaction was completed, an organic layer was isolated and concentrated, and then isolated by column chromatography using hexane, thereby obtaining 22.1 g (yield: 98%) of 2-(2′-nitrophenyl)-thiophene (A′).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541736B2
Source datasetuspto-grants-2009_06
ORD IDord-9694b2f7e6304b59a02c513545c1e0f3
Source noteuspto-grants-2009_06