Technology Process of 4-(o-chlorophenyl)-4-dimethylaminocyclohexanone, ethylene ketal
There total 6 articles about 4-(o-chlorophenyl)-4-dimethylaminocyclohexanone, ethylene ketal which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 89 percent / TsOH / benzene / 6 h / Heating
2: 77 percent / NaOH / ethane-1,2-diol / 18 h / Heating
3: 84 percent / Et3N, (C6H5O)2PON3 / various solvent(s) / 2 h / 90 °C
4: 96 percent / LiAlH4 / tetrahydrofuran / 4 h / Heating
5: 2.) NaBH4 / 1.) H2O, MeOH, reflux, 4 h, 2.) H2O, MeOH, RT, 2 h
With
sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; diphenyl phosphoryl azide; toluene-4-sulfonic acid; triethylamine;
In
tetrahydrofuran; ethylene glycol; benzene;
DOI:10.1021/jm00178a014
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 80 percent / aq. H2SO4 / acetic acid / 24 h / Heating
2: 89 percent / TsOH / benzene / 6 h / Heating
3: 77 percent / NaOH / ethane-1,2-diol / 18 h / Heating
4: 84 percent / Et3N, (C6H5O)2PON3 / various solvent(s) / 2 h / 90 °C
5: 96 percent / LiAlH4 / tetrahydrofuran / 4 h / Heating
6: 2.) NaBH4 / 1.) H2O, MeOH, reflux, 4 h, 2.) H2O, MeOH, RT, 2 h
With
sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; sulfuric acid; diphenyl phosphoryl azide; toluene-4-sulfonic acid; triethylamine;
In
tetrahydrofuran; ethylene glycol; acetic acid; benzene;
DOI:10.1021/jm00178a014
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 77 percent / NaOH / ethane-1,2-diol / 18 h / Heating
2: 84 percent / Et3N, (C6H5O)2PON3 / various solvent(s) / 2 h / 90 °C
3: 96 percent / LiAlH4 / tetrahydrofuran / 4 h / Heating
4: 2.) NaBH4 / 1.) H2O, MeOH, reflux, 4 h, 2.) H2O, MeOH, RT, 2 h
With
sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; diphenyl phosphoryl azide; triethylamine;
In
tetrahydrofuran; ethylene glycol;
DOI:10.1021/jm00178a014