α-Aethyl-cyclohexanaethanol

Base Information

Chemical Name:α-Aethyl-cyclohexanaethanol
CAS No.:33204-52-3
Molecular Formula:C₁₀H₂₀O
Molecular Weight:156.268
Hs Code.:

Synonyms:α-Aethyl-cyclohexanaethanol

Suppliers and Price of α-Aethyl-cyclohexanaethanol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of α-Aethyl-cyclohexanaethanol

Chemical Property:

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Technology Process of α-Aethyl-cyclohexanaethanol

There total 9 articles about α-Aethyl-cyclohexanaethanol 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:

Reference yield: 83.0%

: 36613-93-1
2-Cyclohexyl-butyric acid methyl ester

: 33204-52-3
α-Aethyl-cyclohexanaethanol

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane; toluene; at 0 - 20 ℃;
DOI:10.1021/jo0347011

Reference yield: 77.0%

: 1375390-01-4
C₁₆H₃₁O₅P

: 33204-52-3
α-Aethyl-cyclohexanaethanol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; dichloromethane; at 0 - 20 ℃; for 12h; Cooling with ice; Inert atmosphere;
DOI:10.1055/s-0031-1290485

Reference yield:

: 695-12-5,25498-06-0
vinylcyclohexane

: 97-93-8
triethylaluminum

: 139592-41-9
(2R)-2-cyclohexyl-1,4-butanediol

: 33204-52-3
α-Aethyl-cyclohexanaethanol

: 139592-42-0
(2S)-2-cyclohexylbutane-1,4-diol

Guidance literature:: vinylcyclohexane; triethylaluminum; With (p-S)(p-S)-bis[η⁵-[1-[(1S,2S,5R)-2-isopropyl-5-methylcyclohexyl]indenyl]]zirconium dichloride; In benzene; at 22 ℃; for 24h; Inert atmosphere; Schlenk technique;

With oxygen; In benzene; at 0 ℃; for 26h;

With hydrogenchloride; water; In benzene; at 0 ℃; enantioselective reaction;
DOI:10.1016/j.jorganchem.2012.10.021