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1,1''-[thiophene-2,5-diylbis(hydroxymethylene)]bis[2-[(cyclohexylmethylamino)methyl]ferrocene]

Base Information Edit
  • Chemical Name:1,1''-[thiophene-2,5-diylbis(hydroxymethylene)]bis[2-[(cyclohexylmethylamino)methyl]ferrocene]
  • CAS No.:1192236-59-1
  • Molecular Formula:C42H54Fe2N2O2S
  • Molecular Weight:762.663
  • Hs Code.:
  • Mol file:1192236-59-1.mol
1,1''-[thiophene-2,5-diylbis(hydroxymethylene)]bis[2-[(cyclohexylmethylamino)methyl]ferrocene]

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Chemical Property of 1,1''-[thiophene-2,5-diylbis(hydroxymethylene)]bis[2-[(cyclohexylmethylamino)methyl]ferrocene] Edit
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Technology Process of 1,1''-[thiophene-2,5-diylbis(hydroxymethylene)]bis[2-[(cyclohexylmethylamino)methyl]ferrocene]

There total 1 articles about 1,1''-[thiophene-2,5-diylbis(hydroxymethylene)]bis[2-[(cyclohexylmethylamino)methyl]ferrocene] 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:
With n-butyllithium; N,N,N,N,-tetramethylethylenediamine; ammonium chloride; In tetrahydrofuran; hexane; (under Ar, in dark); thiophene added to soln. of butyllithium and N,N,N',N'-tetramethylethane-1,2-diamine in hexane, refluxed for 2 h, cooled toroom temp., added dropwise to soln. of Fe-complex in THF at 0°C, warmed to room temp.; aq. NH4Cl added, aq. phase extd. with Et2O, organic phase washed with H2O, brine, dried over MgSO4, concd., SiO2 column chromy. with Et2O/hexane;
DOI:10.1002/hlca.200800461
Guidance literature:
With 2,3-dicyano-5,6-dichloro-p-benzoquinone; boron trifluoride diethyl etherate; In dichloromethane; (under Ar, in dark); ligand and Fe-complex in CH2Cl2 degassed for 20 min, 4,5-dichloro-3,6-dioxocyclohexa-1,4-diene-1,2-dicarbonitrile added, BF3*(CH3CH2)2O added, refluxed for 1 h, cooled; concd., residue dissolved in CH2Cl2, basic Al2O3 chromy. eluted with CH2Cl2, collected, ppt. washed with acetone, recrystd. from CH2Cl2/MeOH; elem. anal.;
DOI:10.1002/hlca.200800461
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