Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404591Generated: October 28, 2026

Triethylamine → HCID 66676088, compound

https://huagongshe.com/reaction/404591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-Bromo-4-tert-butyl-5-nitroanilineHCID 57482696—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 66676088HCID 6667608886.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of 2-bromo-4-tert-butyl-5-nitro-phenylamine (27.3 g, 100 mmol) in toluene (200 mL) and water (100 mL) was added Et3N (27.9 mL, 200 mmol), Pd(PPh3)2Cl2 (2.11 g, 3 mmol), CuI (950 mg, 0.5 mmol) and trimethylsilyl acetylene (21.2 mL, 150 mmol) under a nitrogen atmosphere. The reaction mixture was heated at 70° C. in a sealed pressure flask for 2.5 h., cooled to room temperature and filtered through Celite®. The filter cake was washed with EtOAc. The combined filtrate was washed with 5% NH4OH solution and water, dried over Na2SO4 and concentrated. The crude product was purified by column chromatography (0-10% EtOAc/petroleum ether) to provide 4-tert-butyl-5-nitro-2-trimethylsilanylethynylphenylamine as a brown viscous liquid (25 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748612B2
Source datasetuspto-grants-2014_06
ORD IDord-d36754a525aa49d283d1435a579e870c
Source noteuspto-grants-2014_06