Technology Process of 2-((R)-2,2,6-Trimethyl-cyclohexyl)-ethanol
There total 4 articles about 2-((R)-2,2,6-Trimethyl-cyclohexyl)-ethanol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 100 percent / LiAlH4 / CH2Cl2 / 20 h / Ambient temperature
2: 98 percent / NEt3 / CH2Cl2 / 20 h / Ambient temperature
3: 1. n-butyllithium, N,N,N',N'-tetramethylethylendiamine / 1. n-hexane, 1,2-dimethoxyethane, 2 h, room temperature 2. 20 h, room temperature
4: 1. Li, t-BuOH 2. 48percent aq. HF / 1. -78 deg C, THF, 1 h 2. acetonitrile, 1 h, room temperature
With
lithium aluminium tetrahydride; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; hydrogen fluoride; lithium; triethylamine; tert-butyl alcohol;
In
dichloromethane;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 98 percent / NEt3 / CH2Cl2 / 20 h / Ambient temperature
2: 1. n-butyllithium, N,N,N',N'-tetramethylethylendiamine / 1. n-hexane, 1,2-dimethoxyethane, 2 h, room temperature 2. 20 h, room temperature
3: 1. Li, t-BuOH 2. 48percent aq. HF / 1. -78 deg C, THF, 1 h 2. acetonitrile, 1 h, room temperature
With
n-butyllithium; N,N,N,N,-tetramethylethylenediamine; hydrogen fluoride; lithium; triethylamine; tert-butyl alcohol;
In
dichloromethane;
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 1. n-butyllithium, N,N,N',N'-tetramethylethylendiamine / 1. n-hexane, 1,2-dimethoxyethane, 2 h, room temperature 2. 20 h, room temperature
2: 1. Li, t-BuOH 2. 48percent aq. HF / 1. -78 deg C, THF, 1 h 2. acetonitrile, 1 h, room temperature
With
n-butyllithium; N,N,N,N,-tetramethylethylenediamine; hydrogen fluoride; lithium; tert-butyl alcohol;