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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82466Generated: October 26, 2026

Water → Methyl 1-amino-4-(4-chlorobenzyl)-2-naphthoate

https://huagongshe.com/reaction/82466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantMethyl 1-amino-4-bromo-2-naphthoate hydrobromideHCID 66979039—
ReactantHCID 178478124HCID 178478124—
CatalystHCID 178418851HCID 178418851—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 1-amino-4-(4-chlorobenzyl)-2-naphthoateHCID 67031942—

Reaction Steps

To a solution of methyl 1-amino-4-bromo-2-naphthoate hydrobromide (1.94 g, 5.37 mmol) in 10 mL of THF at 0° C. under an atmosphere of nitrogen was added (2-chloro-5-pyridyl)methylzinc chloride (41.6 mL, 0.5 M in THF, 83.2 mmol) and bis(tri-tert-butylphosphine)palladium(0) (0.177 g, 0.346 mmol). The reaction was warmed to rt, and after 16 h, treated with water (10 mL). The mixture was diluted dichloromethane and water, and a beige solid was removed via filtration. The filtrate was extracted 2× with dichloromethane and the combined organic fractions were dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified via silica gel chromatography, eluting with 0-20% ethyl acetate in hexanes provide methyl 1-amino-4-(4-chlorobenzyl)-2-naphthoate that gave a proton NMR spectra consistent with theory and a mass ion (ES+) of 326.1 for [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846702B2
Source datasetuspto-grants-2014_09
ORD IDord-286af83c7eae4a06b3c0512b878b29de
Source noteuspto-grants-2014_09