1-tert-butylacetyl-2-phenyl-imidazoline-4-carboxylic acid tert-butyl ester

Base Information

Chemical Name:1-tert-butylacetyl-2-phenyl-imidazoline-4-carboxylic acid tert-butyl ester
CAS No.:1181818-66-5
Molecular Formula:C₂₀H₂₈N₂O₃
Molecular Weight:344.454
Hs Code.:

Synonyms:1-tert-butylacetyl-2-phenyl-imidazoline-4-carboxylic acid tert-butyl ester

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Chemical Property of 1-tert-butylacetyl-2-phenyl-imidazoline-4-carboxylic acid tert-butyl ester

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Technology Process of 1-tert-butylacetyl-2-phenyl-imidazoline-4-carboxylic acid tert-butyl ester

There total 1 articles about 1-tert-butylacetyl-2-phenyl-imidazoline-4-carboxylic acid tert-butyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 64.0%

: 1181818-61-0
1-t-butylacetyl-2-phenyl-imidazoline-4-carboxylic acid methyl ester

: 75-65-0
tert-butyl alcohol

: 1181818-66-5
1-tert-butylacetyl-2-phenyl-imidazoline-4-carboxylic acid tert-butyl ester

Guidance literature:: 1-t-butylacetyl-2-phenyl-imidazoline-4-carboxylic acid methyl ester; With trimethylaluminum; In toluene; at -78 ℃; for 0.5h; Inert atmosphere;

tert-butyl alcohol; In toluene; at 20 ℃; Inert atmosphere; Reflux;
DOI:10.1021/ol9013552

Reference yield: 79.0%

: 1181818-66-5
1-tert-butylacetyl-2-phenyl-imidazoline-4-carboxylic acid tert-butyl ester

: 100-39-0
benzyl bromide

: 1-t-butylacetyl-4-benzyl-2-phenyl-imidazoline-4-carboxylic acid t-butyl ester

Guidance literature:: With (11bS,11b’S)-2,6-bis(3,4,5-trifluorophenyl)-3,3’,5,5’-tetrahydro-4,4’-spirobi[dinaphtho[2,1-c:1’,2’-e]azepin]-4-ium bromide; potassium hydroxide; In toluene; at 0 ℃; for 5h; optical yield given as %ee; enantioselective reaction;
DOI:10.1021/ol9013552