Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239205Generated: October 29, 2026

m-Toluidine → 1292285-22-3

https://huagongshe.com/reaction/239205

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-ToluidineHCID 7934—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantSodium t-butoxideHCID 23676156—
Reactant9-(3-Bromophenyl)-9-phenyl-9H-fluoreneHCID 58233549—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product1292285-22-3HCID 6669179282%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a 200 mL three-neck flask were put 3.2 g (8.1 mmol) of 9-(3-bromophenyl)-9-phenylfluorene and 2.3 g (24.1 mmol) of sodium tert-butoxide. The air in the flask was replaced with nitrogen. To this mixture were added 40.0 mL of toluene, 0.9 mL (8.3 mmol) of m-toluidine, and 0.2 mL of a 10% hexane solution of tri(tert-butyl)phosphine. The temperature of this mixture was set to 60° C., and 44.5 mg (0.1 mmol) of bis(dibenzylideneacetone)palladium(0) was added to the mixture. The temperature of the mixture was raised to 80° C., followed by stirring for 2.0 hours. After the stirring, the mixture was suction-filtered through Florisil, Celite, and alumina to give a filtrate. The filtrate was concentrated to give a solid, which was then purified by silica gel column chromatography (the developing solvent has a 1:1 ratio of hexane to toluene). Accordingly, 2.8 g of a white solid was obtained in 82% yield, which was the substance to be produced. The synthesis scheme of this Step 1 is shown in the following (E13-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642190B2
Source datasetuspto-grants-2014_02
ORD IDord-5e5572810540424989d6fb8250429169
Source noteuspto-grants-2014_02