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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736117Generated: October 25, 2026

Tri-o-tolylphosphine → 4-(2-Chloro-4-trifluoromethylphenyl)piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/736117

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—
Product4-(2-Chloro-4-trifluoromethylphenyl)piperazine-1-carboxylic acid tert-butyl esterHCID 5348551810%

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 numberUS07595314B2
Source datasetuspto-grants-2009_09
ORD IDord-76b19fc017a945dbb8eb74112f1ddbd5
Source noteuspto-grants-2009_09