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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869610Generated: October 31, 2026

2-(Di-tert-butylphosphino)biphenyl → HCID 86721469, compound

https://huagongshe.com/reaction/869610

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantDimethylamine tetrahydrofuranHCID 22320367—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 86721470HCID 86721470—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 86721469HCID 8672146930.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

(E)-2-{8-[(8-bromo-2-cyclopropylimidazo[1,2-a]pyridin-3-yl)methyl]-3-fluorodibenzo[b,e]oxepin-11(6H)-ylidene}propanenitrile (0.36 g, 0.69 mmol) obtained in Reference Example 14C, step 4 was dissolved in toluene (14 mL), Pd2(dba)3 (0.13 g, 0.14 mmol), 2-(di-tert-butylphosphino)biphenyl (0.04 g, 0.14 mmol), sodium tert-butoxide (0.13 g, 1.4 mmol) and 2 mol/L dimethylamine THF solution (4.5 mL, 9.0 mmol) were added, and the mixture was stirred with heating at 120° C. for 2.5 hr in an Emrys Optimizer microwave synthesizer. The mixture was filtered through celite, the filtrate was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (heptane/ethyl acetate=100/0 v/v-70/30 v/v) to give the title compound (0.10 g, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969345B2
Source datasetuspto-grants-2015_03
ORD IDord-a230b391a6f644a2815bba7ef8ecf6d2
Source noteuspto-grants-2015_03