52 2 |  | Vol. 52 No. 2 | 2022 4 | Apr 2022 |
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ٙĿЙCϳԭ
ȩ뿵ĺϳɼо |
1, С1, Rt2
1. (yng)I(y)g(sh)W(xu)Ժ tˎW(xu)Ժ (yng) 7120002. W(xu) W(xu)W(xu)Ժ 710119 |
ժҪȩ2a~2oԭքec}uõȩ1a~1o»N1d1e1f1j1l1oa(chn)Y(jng)1H NMRESI-MS_C2-ȩ뿣1aĺϳɞӰ푷Ҫ_ȩ뿵ĺϳɗl飺ϱn}un2a=1.21.0܄״25 淴5 minԓl2-ȩ뿣1aʞ90.8 % |
P(gun)I~ȩϳɹˇY |
ЈD(li)̖TQ463īIRaA¾̖1009-9212202202-0036-03 |
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Synthesis and Characterization of Aldoxime |
WANG Ying1, XU Xiao-na1, MA Hong-zhu2
(1. School of Pharmaceutical & Chemical Engineering, Xianyang Vocational Technical College, Xianyang 712000, China; 2. School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi'an 710119, China) |
AbstractA series of aldoxime compounds 1a~1o were prepared from the reaction of aldehydes 2a~2o with hydroxylamine hydrochloride. Among them, 1d, 1e, 1f, 1j, 1l and 1o are new compounds. The structures of the products were characterized by 1H NMR and ESI-MS. The effect of reaction conditions on the yield of product 1a was investigated as model reaction. The optimal synthesis conditions of compound 1a were as followings: the material ratio of n(hydroxylamine hydrochloride)n(2a) = 1.21.0, the reaction mixture was stirred in methanol for 5 min at 25 ; the yield of 2-nitrobenzaldehyde oxime (1a) was up to 90.8 % under the optimal reaction conditions. |
Key wordsaldoxime; synthetic process; structural characterization |
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ߺ(jin)飺 1977ŮühTʿоЙCϳɻW(xu)W(xu)E-mail:ppsurre@163.com
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ոڣ2022-01-01
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