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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464912Generated: November 3, 2026

Water → HCID 11367272, compound

https://huagongshe.com/reaction/1464912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-IodoanilineHCID 12271—
Reactant3,3-Dimethyl-1-butyneHCID 13512—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 11367272HCID 11367272—

Reaction Conditions

Temperature20 °C

Reaction Steps

1.05 g (1.5 mmol) of bis(triphenylphosphine)palladium(II) chloride and 0.26 g (1.5 mmol) of copper(I) iodide are added to a solution consisting of 5.47 g (25 mmol) of 3-iodoaniline in 40 ml of triethylamine. With ice-cooling, 3.08 g (37.5 mmol) of 3,3-dimethyl-1-butyne are added dropwise such that the temperature remains at 20° C. After the addition has ended, the mixture is stirred at 20° C. for 20 hours. The reaction solution is concentrated under reduced pressure and the residue formed is stirred into 1 l of water. The mixture is then extracted three times with diethyl ether. The combined organic phases are once more washed with water, dried with sodium sulphate and concentrated under reduced pressure. The crude product obtained is purified by silica gel chromatography (mobile phase methylene chloride). This gives 2.70 g (60% of theory) of 3-(3,3-dimethylbut-1-yn-1-yl)aniline having a content of 97% according to HPLC. log P=2.71.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999956B2
Source datasetuspto-grants-2015_04
ORD IDord-28c2722fe6c3444897517512ec8b3cf4
Source noteuspto-grants-2015_04