92534-69-5

基本信息
1-甲基-4-硝基-吡唑-5-甲酸
1-甲基-4-硝基-1H-吡唑-5-羧酸
TIMTEC-BB SBB000165
ART-CHEM-BB B000133
1-methyl-4-nitro-1H-pyrazole-5-carboxylate
2-methyl-4-nitropyrazole-3-carboxylic acid
1-METHYL-4-NITRO-5-PYRAZOLECARBOXYLIC ACID
1-METHYL-4-NITRO-1H-PYRAZOLE-5-CARBOXYLIC ACID
2-METHYL-4-NITRO-2H-PYRAZOLE-3-CARBOXYLIC ACID
1H-Pyrazole-5-carboxylic acid, 1-methyl-4-nitro-
1-methyl-4-nitro-1H-pyrazole-5-carboxylic acid(SALTDATA: FREE)
物理化學(xué)性質(zhì)
安全數(shù)據(jù)
制備方法

16034-46-1

92534-69-5
以1-甲基-1H-吡唑-5-羧酸為原料合成1-甲基-4-硝基-吡唑-5-甲酸的一般步驟如下:在嚴(yán)格控制溫度的條件下,將發(fā)煙硫酸(1977 mmol)緩慢滴加至發(fā)煙硝酸(777 mmol)中。隨后,分批加入1-甲基-1H-吡唑-5-羧酸(277 mmol),確保反應(yīng)溫度維持在60℃以下。加料完畢后,于相同溫度下持續(xù)攪拌反應(yīng)混合物1小時(shí)。反應(yīng)完成后,將混合物小心倒入碎冰中淬滅,并用乙酸乙酯(300 mL×3)進(jìn)行萃取。合并有機(jī)相,依次用水(250 mL×2)洗滌,并用無(wú)水硫酸鈉干燥。最后,通過(guò)減壓蒸餾除去溶劑,得到1-甲基-4-硝基-吡唑-5-甲酸,為淺黃色固體,產(chǎn)量23.6 g,收率50%。[00251] 1H NMR(400 MHz, DMSO-d6)δ:8.29(1H, s); 3.95(3H, s)。
參考文獻(xiàn):
[1] Chemistry of Heterocyclic Compounds (New York, NY, United States), 1983, vol. 19, # 12, p. 1326 - 1330
[2] Khimiya Geterotsiklicheskikh Soedinenii, 1983, vol. 19, # 12, p. 1676 - 1679
[3] Journal of Organic Chemistry USSR (English Translation), 1984, vol. 20, # 5, p. 976 - 980
[4] Zhurnal Organicheskoi Khimii, 1984, vol. 20, # 5, p. 1073 - 1078
[5] Patent: WO2009/71705, 2009, A1. Location in patent: Page/Page column 39