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C18H25NO5

Base Information Edit
C<sub>18</sub>H<sub>25</sub>NO<sub>5</sub>

Synonyms:C18H25NO5

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C18H25NO5 Edit
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Technology Process of C18H25NO5

There total 2 articles about C18H25NO5 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:
Guidance literature:
N-trimethylsilyl O-tert-butyl carbamate; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 1h;
tert-butyl 2-(3-methoxyphenyl)-2-oxoacetate; In tetrahydrofuran; hexane; at -78 ℃; for 5h;
With chloro-trimethyl-silane; In tetrahydrofuran; hexane; at -78 - 20 ℃; for 2h;
DOI:10.1246/cl.2011.326
Guidance literature:
Multi-step reaction with 2 steps
1.1: triethylamine / dichloromethane / 1 h / 20 °C
2.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -78 °C
2.2: 5 h / -78 °C
2.3: 2 h / -78 - 20 °C
With n-butyllithium; triethylamine; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1246/cl.2011.326
Guidance literature:
With (S)-[3,3’-diphenyl-1,1’-binaphthalen-2,2’-yl]-N-triflyl phosphoramide; In toluene; at -20 ℃; for 4h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ja203901h
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