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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40130Generated: October 25, 2026

3-Methylbut-1-yne → 4-Methoxy-1-(3-methylbut-1-ynyl)-2-nitrobenzene

https://huagongshe.com/reaction/40130

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylbut-1-yneHCID 69019—
Reactant4-Iodo-3-nitroanisoleHCID 292659—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product4-Methoxy-1-(3-methylbut-1-ynyl)-2-nitrobenzeneHCID 59762351—

Reaction Steps

To a solution of 1-iodo-4-methoxy-2-nitrobenzene (Aldrich, 10 g, 35.8 mmol) in Et3N (60 ml) and DMF (6 ml) was added CuI (34 mg, 0.18 mmol), Pd(PPh3)2Cl2 (126 mg, 0.18 mmol), and 3-methyl-1-butyne (5.0 ml, 73.5 mmol). The mixture was stirred at room temperature for 16 h and was concentrated. The resulting mixture was diluted with EtOAc, washed with H2O, brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→15% EtOAc-hexanes) to yield the title compound as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524917B2
Source datasetuspto-grants-2013_09
ORD IDord-b7a226b1c835495eaf8a21b6a00f0eb4
Source noteuspto-grants-2013_09