Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777539Generated: October 25, 2026

Diisopropylethylamine → Methyl 5-(3-fluorobenzyl)picolinate

https://huagongshe.com/reaction/1777539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Fluorophenylboronic acidHCID 2733986—
ReactantMethyl 5-(bromomethyl)pyridine-2-carboxylateHCID 19699469—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 5-(3-fluorobenzyl)picolinateHCID 67974406264.2%

Reaction Steps

A mixture of 3-fluorophenylboronic acid (0.319 g; 2.28 mmol), methyl 5-(bromomethyl)picolinate (0.350 g; 0.230 mmol), tetrakis-(triphenylphosphine)-palladium(0) (0.175; 0.152 mmol) and N,N diisopropylethylamine (0.524 g; 3.04 mmol) in dimethoxyethane (9 mL) and water (3 mL) was irradiated in a microwave oven at 130° C. for 20 minutes. The resulting solution was partitioned between water and ethyl acetate. The organic layer was separated and concentrated under reduced pressure. The crude residue was purified by flash chromatography on silica gel (eluent 1 to 10% ethyl acetate in dichlomethane) to afford 0.149 g (40%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266832B2
Source datasetuspto-grants-2016_02
ORD IDord-194953a6edf845e894921923b3018298
Source noteuspto-grants-2016_02