N-benzyl-N-(cyclohex-2-enyl)-2-iodoacetamide

Base Information

Chemical Name:N-benzyl-N-(cyclohex-2-enyl)-2-iodoacetamide
CAS No.:85539-57-7
Molecular Formula:C₁₅H₁₈INO
Molecular Weight:355.219
Hs Code.:

Synonyms:N-benzyl-N-(cyclohex-2-enyl)-2-iodoacetamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-benzyl-N-(cyclohex-2-enyl)-2-iodoacetamide

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Technology Process of N-benzyl-N-(cyclohex-2-enyl)-2-iodoacetamide

There total 7 articles about N-benzyl-N-(cyclohex-2-enyl)-2-iodoacetamide 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: 92.0%

: 105706-89-6
N-benzyl-2-chloro-N-(cyclohex-2-enyl)acetamide

: 85539-57-7
N-benzyl-N-(cyclohex-2-enyl)-2-iodoacetamide

Guidance literature:: With potassium iodide; In butanone; for 3h; Heating;
DOI:10.1016/S0040-4020(01)91346-8

Reference yield:

: 141330-12-3
N-benzyl-N-(2-cyclohexenyl)amine

: 85539-57-7
N-benzyl-N-(cyclohex-2-enyl)-2-iodoacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / triethylamine / benzene / 2 h / 20 °C

2: 47 percent / NaI / acetone / 15 h / 20 °C

With triethylamine; sodium iodide; In acetone; benzene;
DOI:10.1021/jo020007u

Reference yield:

: 1521-51-3,113667-32-6
rac-3-bromocyclohexene

: 85539-57-7
N-benzyl-N-(cyclohex-2-enyl)-2-iodoacetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / K₂CO₃ / CHCl₃ / 1 h / 20 °C

2: 99 percent / triethylamine / benzene / 2 h / 20 °C

3: 47 percent / NaI / acetone / 15 h / 20 °C

With potassium carbonate; triethylamine; sodium iodide; In chloroform; acetone; benzene;
DOI:10.1021/jo020007u