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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246721Generated: October 30, 2026

Methanol → HCID 21904789, compound

https://huagongshe.com/reaction/1246721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
ReactantPhenyl triflimideHCID 142176—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-[3-(Trifluoromethyl)pyridin-2-yl]piperidin-4-oneHCID 21904751—
ReactantHCID 178418416HCID 178418416—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21904789HCID 21904789—

Reaction Conditions

Temperature80 °C

Reaction Steps

Lithium diisopropyl amide (37.3 mmol) in THF (75 mL) at −78° C. was treated with 1-[3-(trifluoromethyl)pyridin-2-yl]piperidin-4-one (8.30 g, 34.0 mmol) in THF (25 mL) and stirred for 45 minutes. The mixture was treated with solid PhNTf2 (14.0 g, 39.1 mmol), stirred for 1 hour, and concentrated under reduced pressure. The residue was diluted with ethyl acetate:hexanes (1:1), washed with 1N NaOH, dried (Na2SO4), filtered through a silica plug, and the filtrate was concentrated under reduced pressure. The residue, triethylamine (14.2 mL, 102 mmol), and PdCl2(PPh3)2 (0.944 g, 1.34 mmol) were combined in methanol (7.00 mL, 173 mmol) and DMF (100 mL) and saturated with carbon monoxide gas (bubbling 15 minutes). The mixture was heated at 80° C. under a carbon monoxide atmosphere (1 atm) overnight. The mixture was concentrated to half volume, diluted with diethyl ether, washed with water, brine, dried (Na2SO4), filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography (6% ethyl acetate/hexanes) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129235B2
Source datasetuspto-grants-2006_10
ORD IDord-b602bba1299042368083582d15cfbf12
Source noteuspto-grants-2006_10