Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42385Generated: October 26, 2026

N-(3-Methylphenyl)aniline → HCID 58028469, compound

https://huagongshe.com/reaction/42385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Methylphenyl)anilineHCID 14569—
Reactant9-(4-(bicyclo[4.2.0]octa-1(6),2,4-trien-3-yl)butyl)-9-(4-(bicyclo[4.2.0]octa-1,3,5-trien-3-yl)butyl)-2,7-dibromo-9H-fluoreneHCID 58028498—
SolventTolueneHCID 1140—
ProductHCID 58028469HCID 58028469—

Reaction Steps

To an oven-dried three-neck round-bottom flask under nitrogen, were added 600 mL anhydrous toluene, 14.3 g 9-(4-(bicyclo[4.2.0]octa-1(6),2,4-trien-3-yl)butyl)-9-(4-(bicyclo[4.2.0]octa-1,3,5-trien-3-yl)butyl)-2,7-dibromo-9H-fluorene, and 9.2 mL 3-methyldiphenylamine. After the reaction mixture was degassed with strong nitrogen flow for 30 minutes, 6.44 g sodium tert-butoxide, 0.82 g tris(dibenzylideneacetone)dipalladium(0) (Pd2dba3), and 0.54 g tri-tert-butyl phosphine in 15 mL toluene were added. The reaction mixture was heated to reflux. After three hours, the heating was turn off, and the reaction was allowed to cool down to room temperature. The reaction mixture was filter through a Celite/silica gel plug. The product (13.1 g) was purified by flash chromatography using hexane, 1% then 5% ethyl acetate in hexane solution. The structure was confirmed by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08535974B2
Source datasetuspto-grants-2013_09
ORD IDord-b46fee9b76c24f3ca9805eb4a18a6229
Source noteuspto-grants-2013_09