diethyl 2-(2-(ethylamino)-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1H-benzo[d]imidazole-1,3(2H)-dicarboxylate

Base Information

Chemical Name:diethyl 2-(2-(ethylamino)-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1H-benzo[d]imidazole-1,3(2H)-dicarboxylate
CAS No.:1467055-79-3
Molecular Formula:C₂₃H₃₁N₃O₅
Molecular Weight:429.516
Hs Code.:

Synonyms:diethyl 2-(2-(ethylamino)-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1H-benzo[d]imidazole-1,3(2H)-dicarboxylate

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Chemical Property of diethyl 2-(2-(ethylamino)-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1H-benzo[d]imidazole-1,3(2H)-dicarboxylate

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Technology Process of diethyl 2-(2-(ethylamino)-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1H-benzo[d]imidazole-1,3(2H)-dicarboxylate

There total 2 articles about diethyl 2-(2-(ethylamino)-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1H-benzo[d]imidazole-1,3(2H)-dicarboxylate 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: 17.0%

: 208398-74-7
C₁₃H₁₅ClN₂O₄

: 42984-30-5
3-Ethylamino-5,5-dimethyl-2-cyclohexen-1-on

: 1467055-79-3
diethyl 2-(2-(ethylamino)-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1H-benzo[d]imidazole-1,3(2H)-dicarboxylate

Guidance literature:: With triethylamine; In 1,2-dichloro-ethane; at 0 - 20 ℃; for 1.75h; regioselective reaction;
DOI:10.3998/ark.5550190.p008.153

Reference yield:

: 72473-85-9
ethyl 1H-benzimidazole-1-carboxylate

: 1467055-79-3
diethyl 2-(2-(ethylamino)-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1H-benzo[d]imidazole-1,3(2H)-dicarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 20 °C

2: triethylamine / 1,2-dichloro-ethane / 1.75 h / 0 - 20 °C

With triethylamine; In 1,2-dichloro-ethane;
DOI:10.3998/ark.5550190.p008.153