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1-(benzenesulfonyl)-3-(α-hydroxyprenyl)indole

Base Information Edit
  • Chemical Name:1-(benzenesulfonyl)-3-(α-hydroxyprenyl)indole
  • CAS No.:102210-81-1
  • Molecular Formula:C19H19NO3S
  • Molecular Weight:341.431
  • Hs Code.:
  • Mol file:102210-81-1.mol
1-(benzenesulfonyl)-3-(α-hydroxyprenyl)indole

Synonyms:1-(benzenesulfonyl)-3-(α-hydroxyprenyl)indole

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Chemical Property of 1-(benzenesulfonyl)-3-(α-hydroxyprenyl)indole Edit
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Technology Process of 1-(benzenesulfonyl)-3-(α-hydroxyprenyl)indole

There total 6 articles about 1-(benzenesulfonyl)-3-(α-hydroxyprenyl)indole 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 3 steps
1: 34 percent / diethyl ether / 2 h / Ambient temperature
2: 1.) trtra-n-butylammonium bisulfate, 50percent aq. NaOH / 1.) benzene, RT, 5 min, 2.) 0.5 h
3: 83 percent / lithium aluminum hydride / tetrahydrofuran / 1 h / 0 °C
With sodium hydroxide; lithium aluminium tetrahydride; tetra(n-butyl)ammonium hydrogensulfate; In tetrahydrofuran; diethyl ether;
DOI:10.1021/jo00362a031
Guidance literature:
Multi-step reaction with 4 steps
1: 94 percent / bis(triphenylphosphine)nickel dichloride, methylmagnesium iodide / benzene; diethyl ether / 15 h / Heating
2: 34 percent / diethyl ether / 2 h / Ambient temperature
3: 1.) trtra-n-butylammonium bisulfate, 50percent aq. NaOH / 1.) benzene, RT, 5 min, 2.) 0.5 h
4: 83 percent / lithium aluminum hydride / tetrahydrofuran / 1 h / 0 °C
With sodium hydroxide; bis(triphenylphosphine)nickel(II) chloride; lithium aluminium tetrahydride; methyl magnesium iodide; tetra(n-butyl)ammonium hydrogensulfate; In tetrahydrofuran; diethyl ether; benzene;
DOI:10.1021/jo00362a031
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) tetra-n-butylammonium bisulfate, 50percent KOH / 1.) benzene, 5 min, 2.) 2 h
2: 1.) a) tert-butyllithium, b) cuprous cyanide / 1.) pentane, THF-Et2O 3:1, a) -95 deg C, 6 min, b) 3 min, 2.) a) -95 deg C, 0.5 h, b) -78 deg C, 1 h, c) RT, 14 h
3: 83 percent / lithium aluminum hydride / tetrahydrofuran / 1 h / 0 °C
With potassium hydroxide; lithium aluminium tetrahydride; tert.-butyl lithium; tetra(n-butyl)ammonium hydrogensulfate; copper(l) cyanide; In tetrahydrofuran;
DOI:10.1021/jo00362a031
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