Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091639Generated: October 25, 2026

Triethylamine → N-(3,4-diaminophenyl)-2-(diethylamino)acetamide

https://huagongshe.com/reaction/1091639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-oneHCID 4293995—
Reactant2-Nitro-4-phenylenediamineHCID 4338370—
ReactantGlycine, N,N-diethyl-, sodium salt (1:1)HCID 23670834—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventAcetonitrileHCID 6342—
ProductN-(3,4-diaminophenyl)-2-(diethylamino)acetamideHCID 66593690—

Reaction Steps

2-Nitrobenzene-1,4-diamine (1.55 g, 10.1 mmol), N,N-diethylglycine sodium salt (1.61 g, 10.6 mmol) and DEPBT (3.02 g, 10.0 mmol) were suspended in acetonitrile (75 mL). Triethylamine (2.8 mL, 20.0 mmol) was added and the solution stirred overnight at room temperature. The brown precipitate which was formed was filtered and discarded. The filtrate was concentrated and the residue partitioned between EA and saturated aqueous sodium bicarbonate. The organic phase was washed with water and then with brine, dried over sodium sulfate, and the solvent removed under reduced pressure. The residue was dissolved in ethanol (50 mL) and hydrogenated at atmospheric pressure with 10% palladium on charcoal (1.0 g, 0.9 mmol) at room temperature overnight. Filtration and concentration under reduced pressure gave N-(3,4-diaminophenyl)-2-(diethylamino)acetamide as a light brown semi-solid, which solidified and turned blue on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129396B2
Source datasetuspto-grants-2012_03
ORD IDord-bd23b24b0e704bdcb05f4b922f251601
Source noteuspto-grants-2012_03