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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670164Generated: October 30, 2026

Tris(1,1-dimethylethyl)phosphine → 8,9-Dihydrocyclopenta[def]phenanthrene

https://huagongshe.com/reaction/1670164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactant2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthreneHCID 12524367—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product8,9-Dihydrocyclopenta[def]phenanthreneHCID 605749—

Reaction Steps

The compound 2 (0.65 g, 1.747 mmol), bis(4-biphenyl)amine (TCI Corp.) (1.40 g, 4.37 mmol), sodium tert-butoxide (0.51 g, 0.5 mmol), Pd2(dba)3 [(tris(dibenzylidene acetone) dipalladium(0))] (0.08 g, 0.087 mmol), and tri(tert-butyl)phosphine (0.017 g, 0.087 mmol) in a 50 ml round bottom flask were dissolved with toluene (10 mL), and the reaction mixture was refluxed for 12 hours. After the reaction was terminated, the reaction solution was cooled to room temperature and extracted with distilled water (100 ml). The combined organic layers were dried over MgSO4, concentrated, and purified by silica gel column chromatography. The eluate was concentrated and dried to give a material 1 represented by Formula 9 (1.1 g, yield: 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07990053B2
Source datasetuspto-grants-2011_08
ORD IDord-7dfb347a19a842f3a2ec2013bd9e2c69
Source noteuspto-grants-2011_08