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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358952Generated: October 29, 2026

Triethylamine → N-tert-butyl-N-ethoxalyl-2-nitroaniline

https://huagongshe.com/reaction/358952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthoxalyl chlorideHCID 20884—
ReactantN-tert-Butyl-2-nitroanilineHCID 10797892—
SolventTetrahydrofuranHCID 8028—
ProductN-tert-butyl-N-ethoxalyl-2-nitroanilineHCID 20065638—

Reaction Steps

To a stirred solution of 2-nitro-N-tert-butylaniline (37 g) and triethylamine (35 ml) in tetrahydrofuran (400 ml) was added dropwise a solution of ethoxalyl chloride (25 ml) in tetrahydrofuran (50 ml). The mixture was then brought to reflux temperature for 8 h. The solvent was removed by evaporation, and the residue was partitioned between ether (300 ml) and water (500 ml). The organic phase was washed twice with water, dried over Na2SO4 and evaporated. This left the title compound as light yellow crystals, m.p. 73°-74° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04999353
Source datasetuspto-grants-1991_03
ORD IDord-231e8e5054254f97a84ddcc59e54f853
Source noteuspto-grants-1991_03