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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154536Generated: October 30, 2026

Diethyl Oxalate → Ethyl (6-methoxynaphthalen-2-yl)(oxo)acetate

https://huagongshe.com/reaction/1154536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant2-Bromo-6-methoxynaphthaleneHCID 78786—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178506655HCID 178506655—
ProductEthyl (6-methoxynaphthalen-2-yl)(oxo)acetateHCID 20433897—

Reaction Steps

2-Bromo-6-methoxynaphthalene was converted to the 2-lithio derivative by reaction with n-butyllithium. Diethyl oxalate was then reacted with the 2-lithio-6-methoxynaphthalene to afford ethyl α-keto-6-methoxy-naphth-2-ylacetate. The latter compound was reacted with hydroxylamine hydrochloride and sodium acetate to provide ethyl α-hydroxyimino-6-methoxynaphth-2-ylacetate. A solution of 17.55 g of the oxime in 600 ml of methanol containing 5.3 g of zinc metal dust and 135 ml of 50% (v/v) aqueous formic acid was stirred at 0° C. for three hours. After filtering the reaction mixture, the solvent was removed by evaporation to give 10.3 g of ethyl α-amino-α-(6-methoxynaphth-2-yl)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490370
Source datasetuspto-grants-1984_12
ORD IDord-641574af0182453da5903db2fb9492fe
Source noteuspto-grants-1984_12