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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772645Generated: November 2, 2026

2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl → HCID 117732274, compound

https://huagongshe.com/reaction/1772645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantSodium t-butoxideHCID 23676156—
Reactant1236861-65-6HCID 58548443—
ReactantHCID 131734675HCID 131734675—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 117732274HCID 117732274—

Reaction Conditions

Temperature120 °C

Reaction Steps

A microwave vial was charged with compound 24d (154 mg, 0.840 mmol), compound 24c (350 mg, 0.700 mmol), sodium tert-butoxide (94.1 mg, 0.980 mmol), Pd2(dba)3 (12.8 mg, 0.0140 mmol), and 2-(dicyclohexylphosphino)-2′,4′,6′-tri-isopropyl-1,1′-biphenyl (26.6 mg, 0.0560 mmol) and purged with Argon gas. Toluene (3 mL) was then added and the resulting mixture was heated in a microwave at 120° C. for 1 h. The reaction mixture was allowed to cool to rt, diluted with water (20 mL) and EtOAc (20 mL). The organic layer was separated, dried over Na2SO4, filtered, and concentrated. The residue obtained was purified by flash column chromatography on silica gel (1:0-1:4 heptane/EtOAc) to obtain compound 24e. Mass Spectrum (LCMS, ESI pos.) Calcd. for C36H41N9O3: 648.3 (M+H). Found 648.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249163B2
Source datasetuspto-grants-2016_02
ORD IDord-21dccb077e2948d5be5e15d6bfd1e3d1
Source noteuspto-grants-2016_02