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HRID 986912作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Sulfuric AcidHCID 1118—
反応物Pivalic acidHCID 6417—
反応物Ammonium PersulfateHCID 62648—
反応物3,6-DichloropyridazineHCID 67331—
触媒Silver NitrateHCID 24470—
溶媒WaterHCID 962—
生成物4-tert-Butyl-3,6-dichloropyridazineHCID 8984653.5%

反応条件

温度70 °C

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06630471B1
出典データセットuspto-grants-2003_10
ORD IDord-885c3d0eabf14797a277326d95d201e0
出典メモuspto-grants-2003_10