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(S)-1′-bromo-2′-(3-methylpent-1-en-3-yl)benzene

Base Information
  • Chemical Name:(S)-1′-bromo-2′-(3-methylpent-1-en-3-yl)benzene
  • CAS No.:1423035-64-6
  • Molecular Formula:C12H15Br
  • Molecular Weight:239.155
  • Hs Code.:
(S)-1′-bromo-2′-(3-methylpent-1-en-3-yl)benzene

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Chemical Property of (S)-1′-bromo-2′-(3-methylpent-1-en-3-yl)benzene
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Technology Process of (S)-1′-bromo-2′-(3-methylpent-1-en-3-yl)benzene

There total 4 articles about (S)-1′-bromo-2′-(3-methylpent-1-en-3-yl)benzene 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:
diethylzinc; With n-butyllithium; C21H35N2O(1+)*F6P(1-); copper(II) bis(trifluoromethanesulfonate); In hexane; ethyl acetate; at 25 ℃; Schlenk technique; Inert atmosphere;
C13H18BrO4P; In hexane; ethyl acetate; at 25 ℃; for 120h; enantioselective reaction; Catalytic behavior; Schlenk technique; Inert atmosphere;
DOI:10.1002/chem.201203969
Guidance literature:
With n-butyllithium; copper(I) trifluoromethanesulfonate benzene complex; (S)-1-(2,6-diisopropylphenyl)-3-(1-hydroxy-4-methylpentan-2-yl)imidazolium hexafluorophosphate; In hexane; ethyl acetate; at 0 - 20 ℃; for 72h; Overall yield = 68 %; Overall yield = 81 mg; enantioselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.joc.6b02888
Guidance literature:
(E)-1’-bromo-2’-(4-bromobut-2-en-2-yl)benzene; With copper(I) thiophene-2-carboxylate; C35H39O7P; In dichloromethane; at 20 ℃; for 0.333333h; Inert atmosphere; Schlenk technique;
ethylmagnesium bromide; In diethyl ether; dichloromethane; at -78 ℃; for 1h; Overall yield = 54 %; enantioselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.organomet.9b00194
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