N-octylbutyramide 在
7,7'dicumenyl peroxide 、 氧气 作用下,
以
neat (no solvent) 为溶剂,
生成 alkaline earth salt of/the/ methylsulfuric acid
参考文献:
名称:
Lanska, Bozena; Postnikov, Ludvig Michailovich; Aleksandrov, Albert Leonidovich, Collection of Czechoslovak Chemical Communications, 1981, vol. 46, # 11, p. 2650 - 2656
Lipase-Catalyzed Syntheses of N-Octyl-Alkylamides in Organic Media
作者:Béatrice Tuccio、Elisée Ferré、Louis Comeau
DOI:10.1016/0040-4039(91)85079-k
日期:1991.6
Various lipases can be used in anhydrous hexane to obtained N-octyl-alkylamides in moderate yields.
可以在无水己烷中使用各种脂肪酶,以中等收率获得N-辛基-烷基酰胺。
Conformation, and Charge Tunneling through Molecules in SAMs
作者:Lee Belding、Samuel E. Root、Yuan Li、Junwoo Park、Mostafa Baghbanzadeh、Edwin Rojas、Priscilla F. Pieters、Hyo Jae Yoon、George M. Whitesides
DOI:10.1021/jacs.0c12571
日期:2021.3.10
and influences the rates of tunneling. When R1 = R2, the rates of CT decrease (up to 6.3×), relative to rates of CT observed through SAMs having the same total chain lengths, or thicknesses, when R1 = H. When R1 ≠ H ≠ R2, there is a weaker correlation (relative to that when R1 = H or R1 = R2) between current density and chain length or monolayer thickness, and in some cases the rates of CT through SAMs
本文证明,构成自组装单层 (SAM) 的分子的分子构象(除了组成和结构外)影响通过它们的电荷隧穿 (CT) 速率,在形式为 Au TS / S( CH 2 ) 2 CONR 1 R 2 //Ga 2 O 3 /EGaIn,其中R 1和R 2是不同长度的烷基链。链的长度 R 1和 R 2选择影响单层中分子的构象和构象均匀性。分子的构象影响单层的厚度(即隧道势垒宽度)及其在±1.0 V 时的整流比。当R 1 = H 时,分子有序且主要以反式扩展构象存在。然而,当R 1是烷基(例如,R 1 ≠H)时,它们的构象不再是全反式延伸的,并且分子采用更多的斜切二面角。构象类型的这种变化降低了构象顺序并影响隧穿速率。当 R 1 = R 2,当 R 1 = H 时,相对于通过具有相同总链长或厚度的 SAM 观察到的 CT 速率,CT 速率降低(高达 6.3 倍)。当 R 1 ≠ H ≠ R 2 时,存在较弱
The Ruthenium Catalyzed<i>N</i>-Alkylation of Amides with Alcohols
作者:Yoshihisa Watanabe、Tetsuo Ohta、Yasushi Tsuji
DOI:10.1246/bcsj.56.2647
日期:1983.9
Amides reacted with primary alcohols in the presence of a catalytic amount of RuCl2(PPh3)3 at 180 °C to give the corresponding N-monoalkyl amides in fairly good yields. Thus, benzamide reacted with 1-octanol to give N-octylbenzamide in 76% yield with excellent product selectivity. Little esterification of amides with alcohols occurred and selectivity to the N-alkylation was high. Most of the amides gave N-monoalkyl amides but no N,N-dialkyl amides. But formamide reacted with 1-butanol to give N,N-dibutylformamide, as well as N-butylformamide, in low yield. RuCl2(PPh3)3 was the most effective catalyst for this reaction and RuHCl(PPh3)3 also had some catalytic activity.
Fe3+-exchanged clay catalyzed transamidation of amides with amines under solvent-free condition
作者:Md. Ayub Ali、S.M.A. Hakim Siddiki、Kenichi Kon、Ken-ichi Shimizu
DOI:10.1016/j.tetlet.2013.12.111
日期:2014.2
Fe3+-exchanged montmorillonite is shown to be an effective and reusable heterogeneous catalyst for the transamidation of various amides and amines under solvent-free condition. The catalyst shows high yields and wide substrate scope. (C) 2014 Elsevier Ltd. All rights reserved.
SOUTHAM, R. M.;WHITING, M. C., J. CHEM. SOC. PERKIN TRANS., 1982, 78, N 5, 597-603