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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480617Generated: November 4, 2026

Potassium Carbonate → HCID 90122616, compound

https://huagongshe.com/reaction/1480617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Trifluoromethyl)pyridine-5-boronic AcidHCID 25134278—
ReactantHCID 86718560HCID 86718560—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 90122616HCID 9012261642.6%

Reaction Conditions

Temperature72 °C

Reaction Steps

A mixture of 6,8-dibromo-3-(tert-butyl)-3,4-dihydro-2H-benzo[e][1,3]oxazine (Intermediate 6) (0.621 g, 1.79 mmol), 6-(trifluoromethyl)pyridine-3-boronic acid [purchased from Frontier Scientific] (1.025 g, 5.37 mmol), and potassium carbonate (1.979 g, 14.3 mmol) in 2-propanol (30 mL) and water (6 mL) was purged with nitrogen for 20 minutes. Tetrakis(triphenylphosphine)palladium (0) (114 mg, 0.099 mmol) was added and the resulting mixture heated at 72° C. for 60 minutes then the cooled reaction mixture concentrated under reduced pressure. The residue was dissolved in ethyl acetate, washed with water, dried (MgSO4), filtered and concentrated under reduced pressure to afford a dark brown oil. The product was purified using flash chromatography on silica eluting with a solvent gradient of 0 to 30% ethyl acetate in hexanes to give a yellow solid. The solid was triturated with 1:1 v/v MTBE/hexane, filtered and then dried at 40° C./4-8 mm Hg to give 2-((tert-butylamino)methyl)-4,6-bis(6-(trifluoromethyl)pyridin-3-yl)phenol (0.358 g) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409893B2
Source datasetuspto-grants-2016_08
ORD IDord-1b062d6300ea448b9c654c59c2504bf5
Source noteuspto-grants-2016_08