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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10556Generated: October 29, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 178419024, compound

https://huagongshe.com/reaction/10556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactant5-Bromo-4-methylisoquinolineHCID 21979882—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 178418966HCID 178418966—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 178419024HCID 178419024—

Reaction Conditions

Temperature120 °C

Reaction Steps

According to the method of Example 15, Step A, the title compound was synthesized from Intermediate 93. That is, under nitrogen atmosphere, a suspension of Intermediate 93 (602 mg), tris(dibenzylideneacetone)dipalladium(0) (124 mg), tri(tert-butyl)phosphine (0.5 ml, Kanto Chemicals), cis-N-(tert-butoxycarbonyl)-1,4-cyclohexanediamine (697 mg) and sodium tert-butoxide (390 mg) in toluene was stirred with heating at 120° C. for 16.5 hours. The reaction mixture was cooled to room temperature and added with ethyl acetate (10 ml), and the insoluble matters were removed by filtration through Celite. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to obtain the title compound (45 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-2ef5bc5c67c04ed392a15b43bd1a3710
Source noteuspto-grants-2006_08