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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32650Generated: October 25, 2026

Tri-o-tolylphosphine → 1-[2-Chloro-4-(trifluoromethyl)phenyl]piperazine

https://huagongshe.com/reaction/32650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri-o-tolylphosphineHCID 80271—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-Chloro-4-iodobenzotrifluorideHCID 2736612—
ReactantSodium t-butoxideHCID 23676156—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product1-[2-Chloro-4-(trifluoromethyl)phenyl]piperazineHCID 4683749610%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 0.5 g (1.6 mmol) of 3-chloro-4-iodobenzotrifluoride 0.7 g (3.8 mmol), N-Boc-piperazine, 41 mg (0.04 mmol) Tris(dibenzylideneacetone)dipalladium chloroform complex, 0.44 g (4.43 mmol) sodium-t-butoxide and 48 mg (0.16 mmol) tri-o-tolylphosphine in 6 ml dioxane was heated overnight at 100° C. The solution was allowed to cool to room temperature, taken up in ether (30 ml) and washed with brine (25 ml). The organic layer was dried over Na2SO4, filtered and the solvent was removed in vacuo. The crude oil was chromatographed over on silica gel: Eluent: Heptane-AcOEt 0-10% over 15 min to provide the title compound (0.06 g, 10%) as a brown oil, MS (m/e): 365.1 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427612B2
Source datasetuspto-grants-2008_09
ORD IDord-81443adcf32b432695227f565089dcc7
Source noteuspto-grants-2008_09