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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425518Generated: October 30, 2026

Diethyl Oxalate → Ethyl 2-(2-(tert-butoxycarbonylamino)-6-methoxyphenyl)-2-oxoacetate

https://huagongshe.com/reaction/425518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantTert-butyl 3-methoxyphenylcarbamateHCID 4935487—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(2-(tert-butoxycarbonylamino)-6-methoxyphenyl)-2-oxoacetateHCID 66642425—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 3-methoxyphenylcarbamate (25.6 g, 0.11 mol) in THF (300 mL) was added n-BuLi (0.25 mol, 1.6 M solution in pentane) at −78° C. The resulted solution was stirred at 0° C. for 3 hours and re-cooled to −78° C. followed by the addition of diethyl oxalate (20.1 g, 0.14 mol). The mixture was stirred at −78° C. for 45 min and at ambient temperature for one hour, and quenched with 1 N HCl. The mixture was extracted with ether. The organic solution was dried over sodium sulfate and filtered. The filtrate was concentrated in vacuo to dryness. The residue was subjected to column chromatography to give 3.70 g (27% based on recovered starting material) of the title compound: MS (ES+) m/z 324.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106087B2
Source datasetuspto-grants-2012_01
ORD IDord-d02b4f1e69dd45cb870f259600216bfd
Source noteuspto-grants-2012_01