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(1,4,7,10,13-pentaoxa-cyclohexadec-15-ylmethyl)-triphenylstannane

Base Information
  • Chemical Name:(1,4,7,10,13-pentaoxa-cyclohexadec-15-ylmethyl)-triphenylstannane
  • CAS No.:948052-79-7
  • Molecular Formula:C30H38O5Sn
  • Molecular Weight:597.339
  • Hs Code.:
(1,4,7,10,13-pentaoxa-cyclohexadec-15-ylmethyl)-triphenylstannane

Synonyms:(1,4,7,10,13-pentaoxa-cyclohexadec-15-ylmethyl)-triphenylstannane

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Chemical Property of (1,4,7,10,13-pentaoxa-cyclohexadec-15-ylmethyl)-triphenylstannane
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Technology Process of (1,4,7,10,13-pentaoxa-cyclohexadec-15-ylmethyl)-triphenylstannane

There total 1 articles about (1,4,7,10,13-pentaoxa-cyclohexadec-15-ylmethyl)-triphenylstannane 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 aibn; In dichloromethane; addn. of 15-methylene-1,4,7,10,13-pentaoxacyclohexadecane and aibn to Ph3SnH; stirring at 70°C for 12 h; cooling to room temp., addn. of CH2Cl2; filtration through Celite; removal of solvent in vac., chromy. with silica gel and CH2Cl2; elution with EtOH; elem. anal.;
DOI:10.1021/om700304p
Guidance literature:
In dichloromethane; byproducts: iodobenzene; addn. in small portions under ice of I2 (1 equiv.) to stirred soln. of (1,4,7,10,13-pentaoxacyclohexadec-15-ylmethyl)triphenylstannane (1 equiv.) in CH2Cl2; stirring overnight; removal of solvent and the iodobenzene in vac.; addn. of CH2Cl2, filtration, evapn. of solvent; crystn., elem. anal.;
DOI:10.1021/om700304p
Guidance literature:
In dichloromethane; byproducts: C6H5Br; addn. dropwise of Br2 in CH2Cl2 to cooled (-55°C) soln. of (1,4,7,10,13-pentaoxacyclohexadec-15-ylmethyl)triphenylstannane in CH2Cl2; warming to room temp. overnight; removal of volatiles in vac.; recrystn. from EtOH; elem. anal.;
DOI:10.1021/om700304p
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