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6-(3-benzylpyrrol-1-yl)-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

Base Information
  • Chemical Name:6-(3-benzylpyrrol-1-yl)-1,3-dihydro-1-hydroxy-2,1-benzoxaborole
  • CAS No.:1615685-32-9
  • Molecular Formula:C18H16BNO2
  • Molecular Weight:289.142
  • Hs Code.:
6-(3-benzylpyrrol-1-yl)-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

Synonyms:6-(3-benzylpyrrol-1-yl)-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

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Chemical Property of 6-(3-benzylpyrrol-1-yl)-1,3-dihydro-1-hydroxy-2,1-benzoxaborole
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Technology Process of 6-(3-benzylpyrrol-1-yl)-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

There total 10 articles about 6-(3-benzylpyrrol-1-yl)-1,3-dihydro-1-hydroxy-2,1-benzoxaborole 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:
phenyl(1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrol-3-yl)methanone; With sodium tetrahydroborate; In tetrahydrofuran; for 0.166667h;
With boron trifluoride diethyl etherate; In tetrahydrofuran; for 2h;
DOI:10.1016/j.ejmech.2014.04.079
Guidance literature:
Multi-step reaction with 8 steps
1.1: triethylamine / 1 h / 0 - 20 °C
2.1: tin(II) chloride dihdyrate / ethyl acetate / 4 h / Reflux
3.1: ethyl acetate / 4 h / Reflux
4.1: lithium borohydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere
5.1: n-butyllithium / tetrahydrofuran / 0.25 h / -78 °C / Inert atmosphere
5.2: 20 °C / Inert atmosphere
6.1: hydrogenchloride / water; tetrahydrofuran / Inert atmosphere
7.1: tin(IV) chloride / dichloromethane / 0.25 h / 20 °C
7.2: 24 h
8.1: sodium tetrahydroborate / tetrahydrofuran / 0.17 h
8.2: 2 h
With hydrogenchloride; sodium tetrahydroborate; lithium borohydride; n-butyllithium; tin(II) chloride dihdyrate; tin(IV) chloride; triethylamine; In tetrahydrofuran; dichloromethane; water; ethyl acetate; 7.1: |Friedel-Crafts Acylation / 7.2: |Friedel-Crafts Acylation;
DOI:10.1016/j.ejmech.2014.04.079
Guidance literature:
Multi-step reaction with 3 steps
1.1: hydrogenchloride / water; tetrahydrofuran / Inert atmosphere
2.1: tin(IV) chloride / dichloromethane / 0.25 h / 20 °C
2.2: 24 h
3.1: sodium tetrahydroborate / tetrahydrofuran / 0.17 h
3.2: 2 h
With hydrogenchloride; sodium tetrahydroborate; tin(IV) chloride; In tetrahydrofuran; dichloromethane; water; 2.1: |Friedel-Crafts Acylation / 2.2: |Friedel-Crafts Acylation;
DOI:10.1016/j.ejmech.2014.04.079
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