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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958752Generated: October 29, 2026

4-Iodoaniline → 4-(Non-1-ynyl) aniline

https://huagongshe.com/reaction/1958752

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodoanilineHCID 10893—
ReactantAmmonium HydroxideHCID 14923—
Reactant1-NonyneHCID 18937—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product4-(Non-1-ynyl) anilineHCID 6874381686%

Reaction Steps

To a mixture of 4-iodoaniline (2.19 g, 10 mmol), CuI (38 mg, 0.2 mmol, 2 mol %) and Pd(PPh3)2Cl2 (70 mg, 0.1 mmol, 1 mol %) under argon was added THF (60 mL), followed by non-1-yne (1.49 g, 12 mmol, 1.2 equiv.). After stirring for 1 min at rt, 0.5 M NH4OH (40 mL) was added dropwise. After addition, the resulting mixture was stirred 0/N at rt. It was extracted with ether (60 mL+30 mL) and combined extracts were dried (Na2SO4) and purified by flash chromatography (eluent: EtOAc/Hex=1:6) to give 4-(non-1-ynyl) aniline as a light yellow oil (1.85 g, 86%). 1H NMR (400 MHz, CDCl3) δ 7.22 (d, 2H, J=8.4 Hz), 6.60 (d, 2H, J=8.4 Hz), 3.65 (s, br, 2H, NH2), 2.38 (t, 2H, J=7.0 Hz), 1.59 (quint, 2H, J=7.2 Hz), 1.44 (quint, 2H, J=6.8 Hz), 1.38-1.25 (m, 6H), 0.90 (t, 3H, J=6.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410150B2
Source datasetuspto-grants-2013_04
ORD IDord-4265148cf0b64dfc86a26000362d8f8e
Source noteuspto-grants-2013_04