Citation:
DAI Peng, XIAO Yunjie, WANG Zeyu, CHEN Shikun, HE Tongsheng, SHEN Yongcun. A New Synthetic Route of N-(3-Aminopropyl) methacrylamide Hydrochloride[J]. Chinese Journal of Applied Chemistry,
;2013, 30(11): 1289-1292.
doi:
10.3724/SP.J.1095.2013.30071
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A new method to prepare N-(3-aminopropyl) methacrylamide hydrochloride(Ⅴ) was introduced. N-(3-Chloropropyl) methacrylamide(Ⅱ),obtained by acylation reaction between 3-chloropropylamine hydrochloride(Ⅰ) and methacrylic anhydride,was transformed via Gabriel method to N-[N'-(methacryl)-3-aminopropyl] phthalimide(Ⅲ) and hydrazinolysis product N-(3-aminopropyl) methacrylamide(Ⅳ) and then hydrochloric acidification to compound Ⅴ. The overall yield of the reaction is about 61.1%. This process does not need to use any expensive amino protection reagent,which can dramatically reduces the cost of raw materials.
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