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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367913Generated: October 30, 2026

Dichloromethane → 5-Phenoxynicotinic acid methyl ester

https://huagongshe.com/reaction/1367913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantPhenylboronic AcidHCID 66827—
ReactantMethyl 5-hydroxypyridine-3-carboxylateHCID 354317—
CatalystCupric acetateHCID 8895—
SolventEthyl AcetateHCID 8857—
Product5-Phenoxynicotinic acid methyl esterHCID 59255174—

Reaction Steps

0.31 g (2 mmol) of 5-hydroxy-nicotinic acid methyl ester, 0.73 g (4 mmol) of copper acetate, ˜1 g of 4 Å molecular sieves and 0.85 g (7 mmol) of phenylboronic acid were combined in a flask charged with 20 mL of DCM and 2.0 mL (14 mmol) of Et3N. This reaction slurry was stirred overnight at r.t. The reaction mixture was then diluted with 200 mL of EtOAc and washed 3 times with 10% K2CO3. The organic layer was then dried with Na2SO4, evaporated and purified by flash column chromatography (EtOAc/hexanes=1:2) to give 5-phenoxy-nicotinic acid methyl ester, which was subsequently hydrolyzed according to general procedure B to give 5-phenoxy-nicotinic acid and used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893267B2
Source datasetuspto-grants-2011_02
ORD IDord-3c45113b836b4b668dfd24cbe08bb802
Source noteuspto-grants-2011_02