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(S)-6-(4-Methoxy-benzyl)-1,4-dimethyl-azepan-4-ol

Base Information
  • Chemical Name:(S)-6-(4-Methoxy-benzyl)-1,4-dimethyl-azepan-4-ol
  • CAS No.:845537-38-4
  • Molecular Formula:C16H25NO2
  • Molecular Weight:263.38
  • Hs Code.:
(S)-6-(4-Methoxy-benzyl)-1,4-dimethyl-azepan-4-ol

Synonyms:

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Chemical Property of (S)-6-(4-Methoxy-benzyl)-1,4-dimethyl-azepan-4-ol
Chemical Property:
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Technology Process of (S)-6-(4-Methoxy-benzyl)-1,4-dimethyl-azepan-4-ol

There total 13 articles about (S)-6-(4-Methoxy-benzyl)-1,4-dimethyl-azepan-4-ol 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 11 steps
1: 96 percent / 2,6-di-tert-butyl-p-cresole, Lipase PS / diisopropyl ether; H2O / 1.5 h / Ambient temperature
2: 97 percent / pyridinium p-tosylate / CH2Cl2 / 3 h / Ambient temperature
3: 82 percent / K2CO3 / methanol; H2O / 1.5 h / Ambient temperature
4: 88 percent / 4-dimethylaminopyridine, pyridine / CH2Cl2 / 15 h
5: 86 percent / dimethylsulfoxide / 24 h / 80 - 90 °C
6: 97 percent / TsOH / methanol / 1.5 h / Ambient temperature
7: 80 percent / aq. 2M-NaOH / 3.5 h / Heating
8: ZnCl2, HCl / ethanol
9: K2CO3, NaI / chlorobenzene / Heating
10: a.) NaH (60percent); 2.) 6N HCl / 1.) mineral oil, xylene, reflux; 2.) reflux
11: LiBr / tetrahydrofuran; diethyl ether / Ambient temperature
With pyridine; hydrogenchloride; dmap; sodium hydroxide; Lipase PS; 2,6-di-tert-butyl-4-methyl-phenol; pyridinium p-toluenesulfonate; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; sodium iodide; lithium bromide; zinc(II) chloride; In tetrahydrofuran; methanol; diethyl ether; ethanol; dichloromethane; di-isopropyl ether; water; dimethyl sulfoxide; chlorobenzene;
DOI:10.3987/COM-95-7232
Guidance literature:
Multi-step reaction with 13 steps
1: 74 percent / 1.) sodium hydride / 1.) mineral oil, THF, r.t., 30 min; 2.) THF, 4 h, reflux
2: 95 percent / LiAlH4 / tetrahydrofuran / 4 h / Heating
3: 96 percent / 2,6-di-tert-butyl-p-cresole, Lipase PS / diisopropyl ether; H2O / 1.5 h / Ambient temperature
4: 97 percent / pyridinium p-tosylate / CH2Cl2 / 3 h / Ambient temperature
5: 82 percent / K2CO3 / methanol; H2O / 1.5 h / Ambient temperature
6: 88 percent / 4-dimethylaminopyridine, pyridine / CH2Cl2 / 15 h
7: 86 percent / dimethylsulfoxide / 24 h / 80 - 90 °C
8: 97 percent / TsOH / methanol / 1.5 h / Ambient temperature
9: 80 percent / aq. 2M-NaOH / 3.5 h / Heating
10: ZnCl2, HCl / ethanol
11: K2CO3, NaI / chlorobenzene / Heating
12: a.) NaH (60percent); 2.) 6N HCl / 1.) mineral oil, xylene, reflux; 2.) reflux
13: LiBr / tetrahydrofuran; diethyl ether / Ambient temperature
With pyridine; hydrogenchloride; dmap; sodium hydroxide; lithium aluminium tetrahydride; Lipase PS; 2,6-di-tert-butyl-4-methyl-phenol; pyridinium p-toluenesulfonate; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; sodium iodide; lithium bromide; zinc(II) chloride; In tetrahydrofuran; methanol; diethyl ether; ethanol; dichloromethane; di-isopropyl ether; water; dimethyl sulfoxide; chlorobenzene;
DOI:10.3987/COM-95-7232
Guidance literature:
Multi-step reaction with 5 steps
1: 80 percent / aq. 2M-NaOH / 3.5 h / Heating
2: ZnCl2, HCl / ethanol
3: K2CO3, NaI / chlorobenzene / Heating
4: a.) NaH (60percent); 2.) 6N HCl / 1.) mineral oil, xylene, reflux; 2.) reflux
5: LiBr / tetrahydrofuran; diethyl ether / Ambient temperature
With hydrogenchloride; sodium hydroxide; sodium hydride; potassium carbonate; sodium iodide; lithium bromide; zinc(II) chloride; In tetrahydrofuran; diethyl ether; ethanol; chlorobenzene;
DOI:10.3987/COM-95-7232
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