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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383793Generated: October 31, 2026

Methyl 5-(3-(trifluoromethyl)phenyl)nicotinate → HCID 66660068, compound

https://huagongshe.com/reaction/383793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-(3-(trifluoromethyl)phenyl)nicotinateHCID 20099856—
SolventMethanolHCID 887—
ProductHCID 66660068HCID 6666006836.7%

Reaction Steps

A solution of methyl 5-[3-(trifluoromethyl)phenyl]nicotinate (190.1 mg) in MeOH (30 ml) was hydrogenated (ca. 4 atm) for 2 days in a Parr low-pressure hydrogenation apparatus with a 5 wt. % Rh on Al2O3 catalyst (121.6 mg) at 90° C. Rh on Al2O3 catalyst was filtered off and the filtrate was concentrated in vacuo. The residue was purified with silica gel column chromatography (eluent: CHCl3/MeOH=98/2˜90/10) to give methyl cis-5-[3-(trifluoromethyl)phenyl]piperidine-3-carboxylate (71.2 mg) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367690B2
Source datasetuspto-grants-2013_02
ORD IDord-95f59ce656494788a705b66b1be1ea88
Source noteuspto-grants-2013_02