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(+/-)-ptilocaulin

Base Information
  • Chemical Name:(+/-)-ptilocaulin
  • CAS No.:88154-76-1
  • Molecular Formula:C15H25N3
  • Molecular Weight:247.384
  • Hs Code.:
(+/-)-ptilocaulin

Synonyms:

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Chemical Property of (+/-)-ptilocaulin
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Technology Process of (+/-)-ptilocaulin

There total 11 articles about (+/-)-ptilocaulin 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 10 steps
1: potassium tert-butoxide / tetrahydrofuran / 96 h / Ambient temperature
2: 87 percent / tetrahydrofuran; hexane / 1 h / -100 - -80 °C
3: 89 percent / TsOH / benzene / 1.5 h / 80 °C
4: 64 percent / benzene / 3 h / Irradiation
5: 1.) lithium tri-sec-butylborohydride, 2.) aq. sodium hydroxide, 30percent hydrogen peroxide / 1.) THF, RT, 12 h, 2.) RT, 2 h
6: 99 percent / imidazole / dimethylformamide / 14 h / Ambient temperature
7: 1.) borane-methyl sulfide, 2.) 3 M aq. NaOH, 30percent hydrogen peroxide / 1.) THF, 6 h, 0 deg C 2.) 50 deg C, 10 h
8: 97 percent / Collins reagent / CH2Cl2 / 0.08 h / Ambient temperature
9: potassium tert-butoxide / tetrahydrofuran; 2-methyl-propan-2-ol / 0.5 h / Ambient temperature
10: benzene / 25 h / Heating
With 1H-imidazole; sodium hydroxide; dimethylsulfide borane complex; Collins oxidation agent; potassium tert-butylate; dihydrogen peroxide; L-Selectride; toluene-4-sulfonic acid; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide; tert-butyl alcohol; benzene;
DOI:10.1021/jo00251a004
Guidance literature:
Multi-step reaction with 7 steps
1: 64 percent / benzene / 3 h / Irradiation
2: 1.) lithium tri-sec-butylborohydride, 2.) aq. sodium hydroxide, 30percent hydrogen peroxide / 1.) THF, RT, 12 h, 2.) RT, 2 h
3: 99 percent / imidazole / dimethylformamide / 14 h / Ambient temperature
4: 1.) borane-methyl sulfide, 2.) 3 M aq. NaOH, 30percent hydrogen peroxide / 1.) THF, 6 h, 0 deg C 2.) 50 deg C, 10 h
5: 97 percent / Collins reagent / CH2Cl2 / 0.08 h / Ambient temperature
6: potassium tert-butoxide / tetrahydrofuran; 2-methyl-propan-2-ol / 0.5 h / Ambient temperature
7: benzene / 25 h / Heating
With 1H-imidazole; sodium hydroxide; dimethylsulfide borane complex; Collins oxidation agent; potassium tert-butylate; dihydrogen peroxide; L-Selectride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; tert-butyl alcohol; benzene;
DOI:10.1021/jo00251a004
Guidance literature:
Multi-step reaction with 6 steps
1: 1.) lithium tri-sec-butylborohydride, 2.) aq. sodium hydroxide, 30percent hydrogen peroxide / 1.) THF, RT, 12 h, 2.) RT, 2 h
2: 99 percent / imidazole / dimethylformamide / 14 h / Ambient temperature
3: 1.) borane-methyl sulfide, 2.) 3 M aq. NaOH, 30percent hydrogen peroxide / 1.) THF, 6 h, 0 deg C 2.) 50 deg C, 10 h
4: 97 percent / Collins reagent / CH2Cl2 / 0.08 h / Ambient temperature
5: potassium tert-butoxide / tetrahydrofuran; 2-methyl-propan-2-ol / 0.5 h / Ambient temperature
6: benzene / 25 h / Heating
With 1H-imidazole; sodium hydroxide; dimethylsulfide borane complex; Collins oxidation agent; potassium tert-butylate; dihydrogen peroxide; L-Selectride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; tert-butyl alcohol; benzene;
DOI:10.1021/jo00251a004
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