2-[2,2-bis(ethylsulfanylcyclohexyl)]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide

Base Information

Chemical Name:2-[2,2-bis(ethylsulfanylcyclohexyl)]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide
CAS No.:259171-96-5
Molecular Formula:C₂₂H₃₅NO₃S₂
Molecular Weight:425.657
Hs Code.:

Synonyms:2-[2,2-bis(ethylsulfanylcyclohexyl)]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide

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Chemical Property of 2-[2,2-bis(ethylsulfanylcyclohexyl)]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide

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Technology Process of 2-[2,2-bis(ethylsulfanylcyclohexyl)]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide

There total 2 articles about 2-[2,2-bis(ethylsulfanylcyclohexyl)]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide 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: 99.0%

: 120-20-7
2-(3,4-dimethoxyphenyl)-ethylamine

: 259171-95-4
2-[2,2-bis((ethylsulfanyl)cyclohexyl)]acetic acid

: 259171-96-5
2-[2,2-bis(ethylsulfanylcyclohexyl)]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide

Guidance literature:: 2-[2,2-bis((ethylsulfanyl)cyclohexyl)]acetic acid; With 1,1'-carbonyldiimidazole; In dichloromethane; at 20 ℃; for 1h;

2-(3,4-dimethoxyphenyl)-ethylamine; at 25 ℃; for 0.5h; Further stages.;
DOI:10.1021/jo991414h

Reference yield:

: 1438-96-6
(2-oxocyclohexyl)acetic acid

: 259171-96-5
2-[2,2-bis(ethylsulfanylcyclohexyl)]-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 68 percent / conc. HCl / 12 h / 20 °C

2.1: 1,1'-carbonyl diimidazole / CH₂Cl₂ / 1 h / 20 °C

2.2: 99 percent / 0.5 h / 25 °C

With hydrogenchloride; 1,1'-carbonyldiimidazole; In dichloromethane; 1.1: Addition / 2.1: Substitution / 2.2: Acylation;
DOI:10.1021/jo991414h