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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64407Generated: October 26, 2026

Tributylphosphine → Methyl 5-[(2-fluorobenzyl)oxy]-6-nitronicotinate

https://huagongshe.com/reaction/64407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant2-Fluorobenzylic alcoholHCID 67969—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 46311154HCID 46311154—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-[(2-fluorobenzyl)oxy]-6-nitronicotinateHCID 86713415—

Reaction Steps

To a solution of 2 g of methyl 5-hydroxy-6-nitronicotinate, 1.62 ml of (2-fluorophenyl)methanol, and 3.99 ml of tributylphosphine in 40 ml of THF was added 2.54 ml of diethyl azodicarboxylate under ice-cooling, followed by stirring for 1 hour under ice-cooling and at room temperature for 2 hours. To the reaction mixture were added water and ethyl acetate to carry out a layer separation operation. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 2.58 g of methyl 5-[(2-fluorobenzyl)oxy]-6-nitronicotinate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447090B2
Source datasetuspto-grants-2016_09
ORD IDord-8b197a627fce4032a7a2214eac100ed8
Source noteuspto-grants-2016_09