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ChemicalBook CAS DataBase List N,N-DI-N-BUTYLACETAMIDE

N,N-DI-N-BUTYLACETAMIDE synthesis

12synthesis methods
N,n-di-n-butylacetamide is derived from the condensation of acetyl chloride and di-n-butylamine.
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Yield: 76.5%

Reaction Conditions:

with triethylamine in chloroform for 2 h;Reflux;

Steps:

2.2 Ligand Synthesis
General procedure: DBAA and DBBA were synthesized through the reaction of acetyl chloride (98%, AlfaAesar) or butyryl chloride (99%, Acros Organics), respectively, in chloroform with equimolardibutylamine (99.5%, Sigma-Aldrich) in the presence of equimolar triethylaminebase (99%, Acros Organics) in a stirred ice bath. The solution was then heated to reflux at the boiling point of chloroform for at least 2 h. The organic product was washed withdeionized water, 10 wt% Na2CO3solution, 1.2 mol·L-1 HCl solution and a final deionizedwater wash. The organic layer was dried over anhydrous Na2SO4,filtered, and the solventwas removed under reduced pressure. Both ligands were > 95% pure. The DBAA yield was76.5%, and the DBBA yield was 81.9%. DBAA 1H NMR (500 MHz, CDCl3):δ 0.68 (m,6H), 1.07 (m, 4H), 1.27 (m, 4H), 1.82 (s, 3H), 2.98 (t, 2H), 3.05 (t, 2H).

References:

Canner, Adam J.;Harwood, Laurence M.;Cowell, Joseph;Babra, Jasraj S.;Brown, Solomon F.;Ogden, Mark D. [Journal of Solution Chemistry,2020,vol. 49,# 1,p. 52 - 67]

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