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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628217Generated: October 27, 2026

Tris(1,1-dimethylethyl)phosphine → N-(1,1'-Biphenyl)-2-yl-N-(9,9-dimethyl-9H-fluoren-2-yl)-9,9'-spirobi(9H-fluoren)-2-amine

https://huagongshe.com/reaction/628217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactant2-Bromo-9,9'-spirobi[9H-fluorene]HCID 15287522—
ReactantSodium t-butoxideHCID 23676156—
ReactantN-((1,1'-Biphenyl)-2-yl)-9,9-dimethyl-9H-fluoren-2-amineHCID 66803057—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductN-(1,1'-Biphenyl)-2-yl-N-(9,9-dimethyl-9H-fluoren-2-yl)-9,9'-spirobi(9H-fluoren)-2-amineHCID 66803019—

Reaction Steps

Tri-tert-butylphosphine (4.4 ml of a 1.0 M solution in toluene, 4.4 mmol), palladium acetate (248 mg, 1.1 mmol) and sodium tert-butoxide (16.0 g, 166 mmol) are added to a solution of biphenyl-2-yl-(9,9-dimethyl-9H-fluoren-2-yl)amine (40.0 g, 111 mmol) and 2-bromo-9,9′-spirobifluorene (56.9 g, 144 mmol) in degassed toluene (500 ml), and the mixture is heated under reflux for 2 h. The reaction mixture is cooled to room temperature, diluted with toluene and filtered through Celite. The filtrate is evaporated in vacuo, and the residue is crystallised from ethyl acetate/heptane. The crude product is extracted in a Soxhlet extractor (toluene) and purified by zone sublimation in vacuo twice (p=3×104 mbar, T=298° C.). Biphenyl-2-yl-(9,9-dimethyl-9H-fluoren-2-yl)-(9,9′-spirobifluoren-2-yl)amine is isolated in the form of a pale-yellow solid (20.4 g, 27% of theory, purity >99.99% according to HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09312495B2
Source datasetuspto-grants-2016_04
ORD IDord-fc92ce0dda664304a0101b5275141113
Source noteuspto-grants-2016_04