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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713461Generated: October 26, 2026

(4-Ethoxy-3-fluorophenyl)boronic acid → 1,1-Dimethylethyl 4-(4-ethoxy-3-fluorobenzoyl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/713461

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Ethoxy-3-fluorophenyl)boronic acidHCID 2782821—
Reactant4-Phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl esterHCID 89375800—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystCuprous 2-thiophenecarboxylateHCID 11194830—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dimethylethyl 4-(4-ethoxy-3-fluorobenzoyl)-1-piperidinecarboxylateHCID 7122678282.6%

Reaction Steps

To a mixture of 4-ethoxy-3-fluorophenylboronic acid (0.86 g, 4.67 mmol), ligand TFP (0.144 g, 0.62 mmol), Pd2dba3 (0.29 g, 0.31 mmol), copper (I) thiophene-2-carboxylate (0.89 g, 4.7 mmol) was added a solution of 4-phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl ester (1.0 g, 3.11 mmol) in 10 mL of THF while purging with N2 at 50° C. After 18 hours the reaction mixture was diluted with ethyl acetate, filtered through celite then concentrated in vacuo. Purification by flash chromatography gave the title compound (0.95 g, 2.57 mmol). MS (ESI) m/z 352.0 (M+H+); HPLC (Novapak 150×3.9 mm C-18 column: mobile phase: 35-90% acetonitrile/water with 0.1% TFA, at 2 mL/min over 2 min.) t 1.42 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181266B2
Source datasetuspto-grants-2015_11
ORD IDord-d0bd7f4aa1404a8b81ccc81c987bd368
Source noteuspto-grants-2015_11