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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038718Generated: November 1, 2026

Diisopropylamine → N,N-Dimethyl-3-(4-nitrophenyl)prop-2-yn-1-amine

https://huagongshe.com/reaction/1038718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
ReactantN,N-DimethylpropargylamineHCID 81643—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystBis(benzonitrile)palladium chlorideHCID 498840—
Solvent1,4-DioxaneHCID 31275—
ProductN,N-Dimethyl-3-(4-nitrophenyl)prop-2-yn-1-amineHCID 2256928489.4%

Reaction Steps

Tri-t-butylphosphine (0.25 M in dioxane, 11.9 ml, 3.0 mmol, 0.2 eq.), 3-dimethylamino-1-propyne (2.2 ml, 20.8 mmol, 1.4 eq.), and diisopropylamine (2.7 ml, 19.3 mmol, 1.3 eq.) are added sequentially to a mixture of 4-bromonitrobenzene (3 g, 14.9 mmol), copper (I) iodide (198 mg, 1.0 mmol, 0.07 eq.), and Pd(PhCN)2Cl2 (570 mg, 1.5 mmol, 0.1 eq.) in dioxane (20 ml), under an argon atmosphere. The resulting mixture is stirred for 22 h at RT and concentrated. The residue is dissolved in EE and water and filtered through a pad of celite. The aqueous layer is separated and extracted with EE. The organic phase is washed with brine, dried (sodium sulfate), filtered and concentrated. Purification of the residue by silica gel column chromatography (DCM/MeOH+1% NH3aq, 95:5) affords 2.72 g of the title compound as a brown oil: ESI-MS: 205.0 [MH]+; tR=2.51 min (purity: 100%, gradient J); TLC: Rf=0.41 (DCM/MeOH+1% NH3aq, 95:5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552002B2
Source datasetuspto-grants-2013_10
ORD IDord-504c0f962e64415bb920b1da9c657b0b
Source noteuspto-grants-2013_10