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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373132Generated: November 2, 2026

4-Butylaniline → HCID 68616059, compound

https://huagongshe.com/reaction/2373132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ButylanilineHCID 7694—
ReactantTrans-4,4'-dibromostilbeneHCID 7020566—
ReactantSodium t-butoxideHCID 23676156—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 68616059HCID 68616059—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of tris(di-benzylideneacetone)dipalladium (Pd2(dba)3) (0.335 g, 0.365 mmol) and bis-(diphenylphosphino)ferrocene (DPPF) (0.294 g, 0.530 mmol) in dry toluene (20 ml) under nitrogen atmosphere was added trans-4,4′-dibromostilbene (10) (2.0 g, 5.91 mmol) at room temperature, and the resultant mixture was stirred for 10 min, sodium tert-butoxide (2.6 g) and 4-n-butyl aniline (1.77 g, 11.83 mmol) were added to this solution and stirred at 90° C. overnight. The solid was collected, washed three times with methanol and ether, and isolated in 68.8% (1.93 g) yield as an NAM-pure product. 1H NMR (CDCl3, 500 MHz) δ ppm: 7.38 (d, J=8.0 Hz, 4H), 7.10 (d, J=8.5 Hz, 4H), 7.03 (d, J=8.0 Hz, 4H), 7.0 (d, J=8.5 Hz, 4H), 6.91 (s, 2H, ═CH), 5.77 (s, 2H, NH), 2.56 (t, J=7.7 Hz, CH2, 4H), 1.59 (m, CH2, 4H), 1.37 (m, CH2, 4H), 0.94 (t, J=7.5Hz, CH3, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459106B2
Source datasetuspto-grants-2008_12
ORD IDord-806025c519304284a704b55dca7b89bd
Source noteuspto-grants-2008_12