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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 326624생성일: 2026년 10월 26일

Water → 2-Bromo-4-ethyl-6-nitroaniline

https://huagongshe.com/reaction/326624

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물BromineHCID 24408—
반응물4-Ethyl-2-nitroanilineHCID 251674—
용매Acetic AcidHCID 176—
생성물2-Bromo-4-ethyl-6-nitroanilineHCID 19973468—

반응 단계

To a solution of 4-ethyl-2-nitroaniline (28 g) in acetic acid (250 ml) was added bromine (9.64 ml) dropwise with stirring at room temperature. The reaction mixture was stirred for 1 hour, poured into water, and extracted with ethyl acetate (3×200 ml). The organic layer was washed with water (3×200 ml), brine (2×100 ml), dried over magnesium sulphate and evaporated to yield 2-bromo-4-ethyl-6-nitroaniline (38 g). This was dissolved in ethanol (200 ml), concentrated sulphuric acid (24 ml) was added dropwise, the mixture heated to reflux and solid sodium nitrate (27 g) added in small amounts over 30 minutes. The reaction mixture was refluxed for a further 1 hour, cooled and poured into ice water. The product was extracted into ethyl acetate which was washed with water (2×100 ml). brine (2×100 ml), dried over magnesium sulphate and evaporated to yield 3-bromo-5-ethyl-nitrobenzene (35.5 g), δ (60 MHz, CDCl3), 1.3 (3H, t, CH3), 2.8 (2H, q, CH2) 7.6 (1H, s, 4-H), 7.9 (1H, s. 6-H) and 8.0 (1H, s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05270309
출처 데이터셋uspto-grants-1993_12
ORD IDord-aa9f3fafa911410989c58ea62640f888
출처 메모uspto-grants-1993_12