Technology Process of cis-/trans-1,3-Bis(mercaptomethyl)cyclohexane
There total 4 articles about cis-/trans-1,3-Bis(mercaptomethyl)cyclohexane which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
sodium sulfide; sulfuric acid;
In
N,N-dimethyl-formamide;
at 70 ℃;
for 3h;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 82.1 percent / H2; (Bu)4N*HSO4 / (norbornadieneRhCl)2 / aq. phosphate buffer; cyclohexane / 24 h / 60 °C / 2585.74 Torr / pH 7.4
2: 90.2 percent / LiAlH4; AlCl3 / diethyl ether / 2 h / 20 °C
3: 77.5 percent / pyridine / 18 h
4: 54.8 percent / Na2S*9H2O; H2SO4 / dimethylformamide / 3 h / 70 °C
With
pyridine; sodium sulfide; lithium aluminium tetrahydride; aluminium trichloride; sulfuric acid; hydrogen; tetra(n-butyl)ammonium hydrogensulfate;
di-μ-chlorobis(norbornadiene)dirhodium(I);
In
phosphate buffer; diethyl ether; cyclohexane; N,N-dimethyl-formamide;
1: Catalytic hydrogenation / 2: Reduction / 3: Tosylation / 4: Substitution;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 90.2 percent / LiAlH4; AlCl3 / diethyl ether / 2 h / 20 °C
2: 77.5 percent / pyridine / 18 h
3: 54.8 percent / Na2S*9H2O; H2SO4 / dimethylformamide / 3 h / 70 °C
With
pyridine; sodium sulfide; lithium aluminium tetrahydride; aluminium trichloride; sulfuric acid;
In
diethyl ether; N,N-dimethyl-formamide;
1: Reduction / 2: Tosylation / 3: Substitution;