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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975958Generated: November 4, 2026

Hydrochloric Acid → (3,5-Bis-trifluoromethyl-benzyl)-methyl-(3-o-tolyl-pyridin-4-ylmethyl)-amine

https://huagongshe.com/reaction/1975958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantN-(3,5-bis(trifluoromethyl)benzyl)-N-methyl-3-o-tolylisonicotinamideHCID 9846661—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(3,5-Bis-trifluoromethyl-benzyl)-methyl-(3-o-tolyl-pyridin-4-ylmethyl)-amineHCID 86756660258.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 0.12 g (0.265 mmol) N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-3-o-tolyl-isonicotinamide in 3 ml tetrahydrofuran 1.6 ml of a 1M solution of BH3 in tetrahydrofuran was added and the reaction mixture stirred for 16 h at 60° C. After addition of 2 ml 3M HCl in ether the reaction mixture was stirred for 3 h at 60° C. The solution was cooled to room temperature and 5 ml 3N sodium hydroxide solution and 10 ml ethyl acetate were added. Stirring was continued for ½ h, the phases separated and the aqueous phase extracted twice with 15 ml ethyl acatate. The combined organic layers were washed with brine, dried (magnesium sulfate) and evaporated. Chromatography of the residue afforded 0.30 g (25%) of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225316B1
Source datasetuspto-grants-2001_05
ORD IDord-f5e4b20a80f54e3b96babfc23aa4bd9c
Source noteuspto-grants-2001_05