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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730846Generated: October 30, 2026

Phenethylamine, m-trifluoromethyl- → HCID 86593831, compound

https://huagongshe.com/reaction/730846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylamine, m-trifluoromethyl-HCID 104223—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantHCID 11606965HCID 11606965—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 86593831HCID 86593831—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of the product from step (a) above (88 mg, 0.14 mmol), 2-(3-trifluoromethylphenyl)ethylamine (45 mg, 0.24 mmol, Trans World Chemicals), tris(dibenzylideneacetone)dipalladium(0) (8 mg, 0.01 mmol, Strem), 2-(di-t-butylphosphino)biphenyl (8 mg, 0.03 mmol, Strem) and sodium-tert-butoxide (31 mg, 0.33 mmol, Aldrich) in toluene (2 mL) was heated at 150° C. in a microwave synthesizer for 14 min. The reaction mixture was cooled to room temperature, diluted with EtOAc (5 mL) and filtered through a Celite® pad. The filtrate was concentrated in vacuo and the residue dissolved in MeOH (4 mL), and purified by preparative HPLC (gradient 0.1% trifluoroacetic acid in acetonitrile) to give the title compound as pale-yellow oil. MS (ESI, pos. ion) m/z: 733 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582761B2
Source datasetuspto-grants-2009_09
ORD IDord-247fa052ea6446c5a12d07401b5b1438
Source noteuspto-grants-2009_09