One Pot Synthesis of Tribenzyl Isocyanurate AITranslate
Abstract AITranslate
In this paper one pot synthesis of tribenzyl isocyanurate from urea was studied. First isocyanuric acid w36 prepared from urea by liquid phase method and was not further separated, and then it continued to react with benzyl chloride and triethylamine to give tribenzyl isocyanurate. The reaction conditions and the effects of several factors on the yield were also discussed.
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1陈国斌,任碧野.异氰尿酸三苄基酯的合成研究[J].精细化工,1997,14(3):44-46. 被引量:8
1陈良壁,李碧婵.微波法合成异氰尿酸三苄基酯[J].南平师专学报,2004,23(2):56-59. 被引量:1
2陈国斌,任碧野.一锅法合成异氰尿酸三苄基酯[J].精细石油化工,1998,15(2):45-47.
3陈国斌,任碧野.异氰尿酸三苄基酯的合成研究[J].精细化工,1997,14(3):44-46. 被引量:8
4李铭新.合成异氰尿酸新工艺[J].辽宁化工,1993,22(3):32-33. 被引量:2
5陈洪璞,曲宏伟,唱兴茂.三(羟乙基)异氰尿酸酯合成[J].炼油与化工,1994,11(1):18-21. 被引量:3
6王景明.异氰尿酸及其衍生物[J].河北化工,1993,16(3):41-44.
7最新专利文摘[J].石油化工,2011,40(8):894-894.
8制备粒状水合碱金属二卤异氰尿酸盐喷涂粒化技术(下)[J].江苏氯碱,1995(4):8-11.
9陆则尧.氯代异氰尿酸类产品的生产与应用[J].中国氯碱,1998(3):22-25. 被引量:1
10陈知清.异氰尿酸三(乙—羟乙)酯的合成[J].太化科技,1990(1):41-43.
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DOI:
Chinese Library Classification Number:TQ225.24[化学工程—有机化工]
Citation Information:
In this paper one pot synthesis of tribenzyl isocyanurate from urea was studied. First isocyanuric acid w36 prepared from urea by liquid phase method and was not further separated, and then it continued to react with benzyl chloride and triethylamine to give tribenzyl isocyanurate. The reaction conditions and the effects of several factors on the yield were also discussed.
quote
| GB/T 7714-2015 | [1] CHEN Guo-bin, REN Bi-ye. One Pot Synthesis of Tribenzyl Isocyanurate[J]. Rare Metals and Cemented Carbides, 1998(1): 40-42. |
| MLA | [1] CHEN Guo-bin, and REN Bi-ye. "One Pot Synthesis of Tribenzyl Isocyanurate." Rare Metals and Cemented Carbides, no. 1, 1998, pp. 40-42. |
| APA | [1] CHEN Guo-bin, & REN Bi-ye. (1998). One Pot Synthesis of Tribenzyl Isocyanurate. Rare Metals and Cemented Carbides(1), 40-42. |
| IEEE | [1] CHEN Guo-bin and REN Bi-ye, "One Pot Synthesis of Tribenzyl Isocyanurate," Rare Metals and Cemented Carbides, no. 1, pp. 40-42, 1998. keywords: {lsocyanuric acid;tribenzyl isocyanurate;one pot sythesis} |
