Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121195Generated: November 2, 2026

3-Hydroxypyridine → 4-(3-Pyridyloxymethyl)2-phenylbenzoic acid methyl ester

https://huagongshe.com/reaction/2121195

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxypyridineHCID 7971—
Reactant18-Crown-6HCID 28557—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantMethyl 4-bromomethyl-2-phenylbenzoateHCID 18474540—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(3-Pyridyloxymethyl)2-phenylbenzoic acid methyl esterHCID 1068709848.4%

Reaction Steps

To a mechanically-stirred 0° C. solution of 3-hydroxypyridine (4.4 g, 46 mmol) in DME (20 mL) was added potassium hexamethyldisilazide (0.5 M in toluene, 88.5 mL, 44 mmol) and the mixture was stirred for 15 minutes. 18-Crown-6 (1.46 g, 5.5 mmol) and a solution of 4-bromomethyl-2-phenylbenzoic acid methyl ester (6.8 g, 22 mmol) in toluene (25 mL) was added and the reaction mixture was vigorously stirred overnight. The reaction mixture was poured into 200 mL of water and the layers were separated. The aqueous phase was extracted with 2 portions of ethyl acetate and the combined organic phases were extracted with water and brine, dried (MgSO4), filtered and concentrated. The resulting oil was purified by flash chromatography (65% ethyl acetate-hexane) to give 4-(3-pyridyloxymethyl)-2-phenylbenzoic acid methyl ester (3.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693123B2
Source datasetuspto-grants-2004_02
ORD IDord-46f1714deabd407f83f5d6ccbca48c2c
Source noteuspto-grants-2004_02