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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475154Generated: October 31, 2026

Tris(furan-2-yl)phosphane → HCID 86633386, compound

https://huagongshe.com/reaction/1475154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(furan-2-yl)phosphaneHCID 521585—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Reactant4,4,4-Trifluoro-1-(4-nitrophenyl)-1,3-butanedioneHCID 11065204—
ReactantHCID 66968518HCID 66968518—
ReactantHCID 86633387HCID 86633387—
CatalystPalladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1)HCID 11029508—
CatalystCopper thiophene-2-carboxylateHCID 15171005—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86633386HCID 8663338641%

Reaction Conditions

Temperature52 °C

Reaction Steps

4-Trifluoromethyl-6-(4-nitrophenyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine. A solution of 4-trifluoromethyl-2-methylsulfanyl-6-(4-nitrophenyl)-pyrimidine (1.25 g, 4.0 mmol, prepared from 1-(4-nitrophenyl-4,4,4-trifluorobutane-1,3-dione according to Green et al. WO 200138311 A2), 4-trifluoromethylphenylboronic acid (0.95 g, 5.0 mmol), trifurylphosphine (140 mg, 0.60 mmol), and copper (II) 2-thiophenecarboxylate (1.05 g, 5.0 mmol) were combined in 25 mL of dry THF and heated to 52° C. The catalyst tris(dibenzyl-ideneacetone)dipalladium(0)-chloroform adduct (100 mg) was then added in three portions over 3 h, and the solution was then allowed to stir at 50° C. for 12 h. Concentration and chromatography (Biotage, 4:1 hexane/DCM) furnished 0.67 g (41%) of the title compound as a light yellow solid. 1H NMR (300 MHz, CDCl3) δ 8.75 (d, J=8 Hz, 2H), 8.41 (s, 4H), 8.03 (s, 1H), 7.80 (d, J=8 Hz, 2H); EIMS 414.1 (M+H); mp 162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018363B2
Source datasetuspto-grants-2015_04
ORD IDord-40167eeebec546d5b8b39150a0d1ede8
Source noteuspto-grants-2015_04