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Synthesis of 1,3,5,5-Tetranitrohexahydropyrimidine with By-product of FOX-7 Prepared by 4,6-Dihydroxy-2-methylpyrimidine
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(1. School of Chemical Engineering Nanjing University of Science and Technology, Nanjing 210094, China; 2. Nanjing No.13 Middle School, Nanjing 210094, China)

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    Abstract:

    By-product dinitromethane in the manufacturing process of 1, 1-diamino-2, 2-dinitroethylene(FOX-7) from 4, 6-dihydroxy-2-methylpyrimidine(MPO) was recovered, the long needle dinitromethane potassium salt(KDNM) crystal with stable property was prepared via neutralization using aqueous potassium hydroxide solution, 1, 3-dibutyl -5, 5-dinitrohexahydropyrimidine was prepared via Mannich condensation reaction using KDNM, formaldehyde and tert-butylamine as raw materials, and 1, 3, 5, 5-tetranitrohexahydropyrimidine(DNNC) was prepared via the nitrolysis of 1, 3-dibutyl -5, 5-dinitrohexahydropyrimidine with mixed acid system of concentrated sulfuric acid and concentrated nitric acid with total yield of 78.9%(Calculated by KDNM). The structure of DNNC and intermediate were characterized by 1H NMR, IR, MS. The effect of pH value, solvents and temperature on Mannich condensation reaction, and the effect of selection of nitration system on the nitating reaction were studied. The optimal conditions of Mannich condensation reaction were determined as: the molar ratio of KDNM, formaldehyde and tert-butylamine is 1.0:3.5:2.0, 10% aqueous methanol solution is used as solvent and hydrochloric acid is used to adjust pH value to 8 at room temperature; and then temperature rises up to 50 ℃ subsequently with reaction for 3 hours, and the yield reaches 85.3%. Using mixed acid composed of 20 mL 98% H2SO4 and 10 mL HNO3By as nitrolysis system, the yield reaches 92.5%.

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朱元玉,杜杨,杜雨昕.2-甲基嘧啶-4,6-二酮制FOX-7的副产物合成1,3,5,5-四硝基六氢嘧啶[J].含能材料,2018,26(4):329-333.
ZHU Yuan-yu, DU Yang, DU Yu-xin. Synthesis of 1,3,5,5-Tetranitrohexahydropyrimidine with By-product of FOX-7 Prepared by 4,6-Dihydroxy-2-methylpyrimidine[J]. Chinese Journal of Energetic Materials,2018,26(4):329-333.

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History
  • Received:May 24,2017
  • Revised:October 26,2017
  • Adopted:
  • Online: April 16,2018
  • Published: April 25,2018