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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091767Generated: November 1, 2026

Methyl 5-[4-(2,2,2-trifluoroethyl)phenyl]nicotinate → Methyl 5-[4-(2,2,2-trifluoroethyl)phenyl]piperidine-3-carboxylate

https://huagongshe.com/reaction/2091767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-[4-(2,2,2-trifluoroethyl)phenyl]nicotinateHCID 58116526—
CatalystPalladiumHCID 23938—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
ProductMethyl 5-[4-(2,2,2-trifluoroethyl)phenyl]piperidine-3-carboxylateHCID 58116537—

Reaction Steps

A solution of 9.20 g (23.4 mmol) of the compound from Example 41A in concentrated acetic acid (192 ml) was admixed with 1.94 g of palladium/carbon (10% palladium) and 2.23 g of platinum(IV) oxide. This was followed by hydrogenation under a hydrogen atmosphere at standard pressure for 6 h, then addition of another 1.00 g of palladium/carbon (10% palladium) and 2.00 g of platinum(IV) oxide, and hydrogenation under a hydrogen atmosphere at standard pressure overnight. Subsequently, a further 1.00 g of palladium/carbon (10% palladium) and 3.00 g of platinum(IV) oxide were added, and hydrogenation was effected under a hydrogen atmosphere at standard pressure for a further 24 h. The reaction solution was filtered through Celite, the filter residue was washed with methanol/water and the combined filtrates were concentrated under reduced pressure. The residue was taken up in dichloromethane and then washed with a 1 N aqueous sodium carbonate solution. The organic phase was dried over sodium sulphate, filtered and concentrated under reduced pressure. Yield: 6.64 g (85% of theory, purity 90%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440657B2
Source datasetuspto-grants-2013_05
ORD IDord-a603bf9324e74e54ac3df655d2adf2b3
Source noteuspto-grants-2013_05