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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969657Generated: October 30, 2026

Sodium Carbonate → 3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-(trifluoromethyl)benzenamine

https://huagongshe.com/reaction/969657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
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—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
Product3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-(trifluoromethyl)benzenamineHCID 21959643—

Reaction Conditions

Temperature80 °C

Reaction Steps

3-(5,5-dimethyl-[1,3,2]dioxaborinan-2-yl)-5-trifluoromethyl-phenylamine (8.8 g, 0.032 mmol) was added to trifluoro-methanesulfonic acid 1-methyl-1,2,3,6-tetrahydro-pyridin-4-yl ester (7.91 g, 0.032 mmol) and 2 N Na2CO3 aqueous solution (25 mL) was bubbled through N2 for 5 min. Pd(PPh3)4 (3.7 g, 3.2 mmol) 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 product was isolated by passing through silica gel column chromatography (EtOAc, then (2 M NH3) in MeOH/EtOAc) to provide a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307088B2
Source datasetuspto-grants-2007_12
ORD IDord-2e677c69b77749e99255c483e6af8fb6
Source noteuspto-grants-2007_12