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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889964Generated: October 30, 2026

Sodium Carbonate → 3-(1-Methyl-1,2,3,4-tetrahydro-pyridin-4-yl)-5-trifluoromethyl-phenylamine

https://huagongshe.com/reaction/889964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
ReactantLithium ChlorideHCID 433294—
Reactant1-Methyl-1,2,3,6-tetrahydropyridin-4-yl trifluoromethanesulfonateHCID 11379577—
Reactant3-(5,5-Dimethyl-[1,3,2]dioxaborinan-2-yl)-5-trifluoromethyl-phenylamineHCID 21959607—
Product3-(1-Methyl-1,2,3,4-tetrahydro-pyridin-4-yl)-5-trifluoromethyl-phenylamineHCID 22249446—

Reaction Conditions

Temperature80 °C

Reaction Steps

3-(5,5-Dimethyl-[1,3,2]dioxaborinan-2-yl)-5-trifluoromethyl-phenylamine (1.2 g) was added to trifluoro-methanesulfonic acid 1-methyl-1,2,3,6-tetrahydro-pyridin-4-yl ester (1.0 g), LiCl (500 mg, Aldrich), PPh3 (300 mg, Aldrich) and 2M Na2CO3 aqueous solution (6 ml) and was bubbled with N2 for 5 min. Pd(PPH3)4 (300 mg, Aldrich) was added and the reaction was heated to 80° C. for 16 h. The reaction was cooled to RT and diluted with Et2O (100 mL). The mixture was filtered through Celite® and the filtrate was washed with NaHCO3 aqueous solution (25 ml) followed by brine (25 mL). The organic phase was dried over Na2SO4 and concentrated in vacuo. The desired compound was isolated by silica gel column chromatography (EtOAc 10% (2M NH3) in MeOH/EtOAc) to provide yellow oil. M+H 257.2; Calc'd 256.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995162B2
Source datasetuspto-grants-2006_02
ORD IDord-9d54dd64dbeb44be92fdb31e6b7bcfac
Source noteuspto-grants-2006_02