25016-02-8

基本信息
2-甲氧基-5-硝基苯甲醛
苯甲醛,2-甲氧基-5-硝基-
5-Nitro-o-anisaldehyde
5-Nitro-o-anisaldehyde
2-METHOXY-5-NITROBENZALDEHYDE
2-methoxy-5-nitro-benzaldehyd
Benzaldehyde, 2-methoxy-5-nitro-
4-(4-morpholinyl)-6-[[4-(phenylmethyl)-1-piperazinyl]methyl]-1,3,5-triazin-2-amine
物理化學性質(zhì)
制備方法

97-51-8

74-88-4

25016-02-8
以5-硝基水楊醛和碘甲烷為原料合成2-甲氧基-5-硝基苯甲醛的一般步驟:向5-硝基水楊醛(1.00g,6.0mmol)的N,N-二甲基甲酰胺(DMF,20ml)溶液中加入氫化鈉(NaH,246mg)和碘甲烷(2.56g)。將反應(yīng)混合物在0℃下攪拌8.5小時。反應(yīng)完成后,用乙醚萃取反應(yīng)混合物,依次用碳酸氫鈉水溶液、飽和食鹽水和5%鹽酸/飽和食鹽水洗滌有機相。有機相用無水硫酸鎂干燥后,減壓濃縮,得到2-甲氧基-5-硝基苯甲醛(0.95g,產(chǎn)率87.8%),為黃色針狀晶體。產(chǎn)物經(jīng)1H NMR(CDCl3)表征:δ 10.45(s,1H),8.70(d,J = 2.9Hz,1H),8.45(dd,J = 8.8, 2.9Hz,1H),7.14(d,J = 8.8Hz,1H),4.08(s,3H)。
參考文獻:
[1] Angewandte Chemie - International Edition, 2011, vol. 50, # 15, p. 3435 - 3438
[2] Patent: US2013/261295, 2013, A1. Location in patent: Paragraph 0166; 0167
[3] Journal of the American Chemical Society, 2017, vol. 139, # 19, p. 6654 - 6662
[4] Patent: US5837711, 1998, A
[5] Journal of the Chemical Society, 1951, p. 2462,2466