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tert-butyl N-[2-[4-(4'-bromo-3',5'-dimethyl[2,2']bithyophen-5-yl)phenoxy]ethyl]-N-methyl carbamate

Base Information
  • Chemical Name:tert-butyl N-[2-[4-(4'-bromo-3',5'-dimethyl[2,2']bithyophen-5-yl)phenoxy]ethyl]-N-methyl carbamate
  • CAS No.:921596-32-9
  • Molecular Formula:C24H28BrNO3S2
  • Molecular Weight:522.527
  • Hs Code.:
tert-butyl N-[2-[4-(4'-bromo-3',5'-dimethyl[2,2']bithyophen-5-yl)phenoxy]ethyl]-N-methyl carbamate

Synonyms:tert-butyl N-[2-[4-(4'-bromo-3',5'-dimethyl[2,2']bithyophen-5-yl)phenoxy]ethyl]-N-methyl carbamate

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Chemical Property of tert-butyl N-[2-[4-(4'-bromo-3',5'-dimethyl[2,2']bithyophen-5-yl)phenoxy]ethyl]-N-methyl carbamate
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Technology Process of tert-butyl N-[2-[4-(4'-bromo-3',5'-dimethyl[2,2']bithyophen-5-yl)phenoxy]ethyl]-N-methyl carbamate

There total 1 articles about tert-butyl N-[2-[4-(4'-bromo-3',5'-dimethyl[2,2']bithyophen-5-yl)phenoxy]ethyl]-N-methyl carbamate 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:
Multi-step reaction with 4 steps
1: 79 percent / Ni(dppp)Cl2 / diethyl ether / 22 h
2: AcONa
3: triisopropyl borate
4: 60 percent / PPh3; aq. Na2CO3 / Pd(dba)2 / tetrahydrofuran / Heating
With 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); Triisopropyl borate; sodium acetate; sodium carbonate; triphenylphosphine; bis(dibenzylideneacetone)-palladium(0); In tetrahydrofuran; diethyl ether;
DOI:10.1002/anie.200602591
Guidance literature:
tert-butyl N-[2-[4-(4'-bromo-3',5'-dimethyl[2,2']bithyophen-5-yl)phenoxy]ethyl]-N-methyl carbamate; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.333333h;
octaperfluorocyclopentene; In tetrahydrofuran; hexane; at 20 ℃; for 6h;
DOI:10.1002/anie.200602591
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