Authors
Harden M McConnell, Roger D Kornberg
Publication date
1971/3/1
Journal
Biochemistry
Volume
10
Issue
7
Pages
1111-1120
Publisher
American Chemical Society
Description
Materials and Methods
Tempocholine (Molecule 11) Chloride. 7V, 7V-Dimethyl-A-(2', 2', 6', 6'-tetramethyl-4'-piperidyl)-2-acetoxyethylammonium bromide was prepared by the reaction of 4-(N, N-dimethylamino)-2, 2, 6, 6-tetramethylpiperidine with 2-bromoethyl acetate and then hydrolyzed, oxidized, and ion ex-changed to tempocholine bicarbonate. An aqueous solution of tempocholinebicarbonate was acidified with HC1 to yield tempocholine chloride. This procedure was partly due to Dr. Wayne L. Hubbell.(a) 4-((V,(V-Dimethylamino)-2, 2, 6, 6-tetramethylpiperidine was prepared by the method of Icke and Wisegarver (1955). 4-Amino-2, 2, 6, 6-tetramethylpiperidine(Aldrich Chemical Co.)(25 g) was added with magnetic stirring to 38 g of 98% formic acid in an ice bath. The mixture was removed from the ice bath, combined with 28.5 g of 37% formaldehyde, refluxed for about 10 hr, cooled in an ice bath, and com …
Total citations
19851986198719881989199019911992199319941995199619971998199920002001200220032004200520062007200820092010201120122013201420152016201720182019202020212022202320242214161311159812121415251113217101124151615213327232117272016173722262021177