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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1091639생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1091639

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-oneHCID 4293995—
반응물2-Nitro-4-phenylenediamineHCID 4338370—
반응물Glycine, N,N-diethyl-, sodium salt (1:1)HCID 23670834—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
용매AcetonitrileHCID 6342—
생성물N-(3,4-diaminophenyl)-2-(diethylamino)acetamideHCID 66593690—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08129396B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-bd23b24b0e704bdcb05f4b922f251601
출처 메모uspto-grants-2012_03