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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713422Generated: October 27, 2026

2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride) → 4-(2-Trifluoromethoxy-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/713422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)HCID 2777204—
Reactantp-Tolylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl esterHCID 117819078—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystCuprous 2-thiophenecarboxylateHCID 11194830—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(2-Trifluoromethoxy-benzoyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 11781888789.9%

Reaction Steps

To a mixture of 2-trifluoromethoxy-phenyl-boronic acid (0.307 g, 2.24 mmol, 1.5 eq.), ligand TFP (0.069 g, 0.298 mmol, 0.2 eq.), Pd2(dba)3 (0.154 g, 0.149 mmol, 0.1 eq.), copper (I) thiophene-2-carboxylate (0.426 g, 2.24 mmol, 1.5 eq.) was added a solution of p-tolylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl ester (0.479 g, 1.49 mmol, 1 eq.) in 15 mL of DME while purging with N2 at room temperature. After 18 h stirring at room temperature, the reaction mixture was diluted with ethyl acetate and filtered through celite. The filtrate was concentrated to give an oil. This oil was purified by silica gel column chromatography (10% ethyl acetate/heptane) to give the title compound as a white solid (0.5 g, 86%). Exact mass calculated for C18H23F3N1O4 374.2. MS (ESI) m/z 274.3 [(M-100)H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181266B2
Source datasetuspto-grants-2015_11
ORD IDord-8d99f16068cc49e6b42a7d85fc6fd027
Source noteuspto-grants-2015_11