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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 986912생성일: 2026년 10월 24일

Ammonia → 4-tert-Butyl-3,6-dichloropyridazine

https://huagongshe.com/ko/reaction/986912

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Sulfuric AcidHCID 1118—
반응물Pivalic acidHCID 6417—
반응물Ammonium PersulfateHCID 62648—
반응물3,6-DichloropyridazineHCID 67331—
촉매Silver NitrateHCID 24470—
용매WaterHCID 962—
생성물4-tert-Butyl-3,6-dichloropyridazineHCID 8984653.5%

반응 조건

온도70 °C

반응 단계

Concentrated sulphuric acid (53.6 ml, 1.0 mol) was added carefully to a stirred suspension of 3,6-dichloropyridazine (50.0 g, 0.34 mol) in water (1.25 l). This mixture was then heated to 70° C. (internal temperature) before the addition of trimethylacetic acid (47.5 ml, 0.41 mol). A solution of silver nitrate (11.4 g, 0.07 mol) in water (20 ml) was then added over approximately one minute. This caused the reaction mixture to become milky in appearance. A solution of ammonium persulphate (230 g, 1.0 mol) in water (0.63 l) was then added over 20-30 minutes. The internal temperature rose to approximately 85° C. During the addition the product formed as a sticky precipitate. Upon complete addition the reaction was stirred for an additional 10 minutes, then allowed to cool to room temperature. The mixture was then poured onto ice and basified with concentrated aqueous ammonia, with the addition of more ice as required to keep the temperature below 10° C. The aqueous was extracted with dichloromethane (3×300 ml). The combined extracts were dried (MgSO4), filtered and evaporated to give 55.8 g of crude product as an oil. This was purified by silica gel chromatography using 0-15% ethyl acetate in hexane as eluent to give 37.31 g (53%) of the desired compound. Data for the title compound: 1H NMR (360 MHz, d6-DMSO) δ1.50 (9H, s), 7.48 (1H, s); MS (ES+) m/e 205 [MH]+, 207 [MH]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06630471B1
출처 데이터셋uspto-grants-2003_10
ORD IDord-885c3d0eabf14797a277326d95d201e0
출처 메모uspto-grants-2003_10