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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842794Generated: November 1, 2026

Binap, (A+-)- → N-(2-(2,2,2-Trifluoroethoxy)phenyl)-4-piperidone propylene ketal

https://huagongshe.com/reaction/842794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant4-Piperidone propylene ketalHCID 12954117—
Reactant1-Bromo-2-(2,2,2-trifluoroethoxy)benzeneHCID 22615479—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
SolventSodium chloride; waterHCID 57417360—
ProductN-(2-(2,2,2-Trifluoroethoxy)phenyl)-4-piperidone propylene ketalHCID 57019377—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 50 (1.786 g, 7.00 mmol) and 4-piperidone propylene ketal (2.645 g, 16.82 mmol) in toluene (30 mL) was treated with sodium tert-butoxide (1.88 g, 19.56 mmol), (S)-BINAP (44 mg, 0.07 mmol), and tris(dibenzylideneacetone)dipalladium(0) (32 mg, 0.035 mmol) at room temperature. The mixture was heated in an oil bath (80° C., 3 h). The mixture was diluted with ether and brine. The aqueous layer was extracted with two additional portions of ether and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated under reduced pressure. PCTLC (SiO2, 6 mm, 20% EtOAc-80% hexane) afforded the title compound (51).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376503B1
Source datasetuspto-grants-2002_04
ORD IDord-fb00847501dd46f78e336a2a664abbff
Source noteuspto-grants-2002_04