Succinic acid mono-((1R,2S,4R)-4-tert-butyl-2-methyl-cyclohexyl) ester; compound with (S)-1-phenyl-ethylamine

Base Information

Chemical Name:Succinic acid mono-((1R,2S,4R)-4-tert-butyl-2-methyl-cyclohexyl) ester; compound with (S)-1-phenyl-ethylamine
CAS No.:85114-34-7
Molecular Formula:C₈H₁₁N*C₁₅H₂₆O₄
Molecular Weight:391.551
Hs Code.:

Synonyms:Succinic acid mono-((1R,2S,4R)-4-tert-butyl-2-methyl-cyclohexyl) ester; compound with (S)-1-phenyl-ethylamine

Suppliers and Price of Succinic acid mono-((1R,2S,4R)-4-tert-butyl-2-methyl-cyclohexyl) ester; compound with (S)-1-phenyl-ethylamine

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of Succinic acid mono-((1R,2S,4R)-4-tert-butyl-2-methyl-cyclohexyl) ester; compound with (S)-1-phenyl-ethylamine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Succinic acid mono-((1R,2S,4R)-4-tert-butyl-2-methyl-cyclohexyl) ester; compound with (S)-1-phenyl-ethylamine

There total 4 articles about Succinic acid mono-((1R,2S,4R)-4-tert-butyl-2-methyl-cyclohexyl) ester; compound with (S)-1-phenyl-ethylamine 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:

: 2484-73-3
cis-2-methyl-trans-4-tert-butylcyclohexanol

: 85114-34-7
Succinic acid mono-((1R,2S,4R)-4-tert-butyl-2-methyl-cyclohexyl) ester; compound with (S)-1-phenyl-ethylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 150 g / pyridine / 2 h / Heating

2: ethyl acetate; methanol

With pyridine; In methanol; ethyl acetate;
DOI:10.1021/ja00348a048

Reference yield:

: 58911-80-1,67009-19-2,67009-20-5,67009-21-6,85114-30-3,114128-98-2,58911-72-1
trans-4-tert-Butyl-2-methyl-cyclohexanone-N,N-dimethylhydrazone

: 85114-34-7
Succinic acid mono-((1R,2S,4R)-4-tert-butyl-2-methyl-cyclohexyl) ester; compound with (S)-1-phenyl-ethylamine

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / m-chloroperbenzoic acid / dimethylformamide / 0.5 h / -63 °C

2: 99 percent / lithium aluminum hydride / diethyl ether / 0.75 h / 0 °C

3: 150 g / pyridine / 2 h / Heating

4: ethyl acetate; methanol

With pyridine; lithium aluminium tetrahydride; 3-chloro-benzenecarboperoxoic acid; In methanol; diethyl ether; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/ja00348a048

Reference yield:

: 3211-27-6,5064-52-8,74365-81-4,74365-82-5,85114-29-0,110415-88-8,3211-26-5,148810-44-0,148810-45-1
4-tert-butyl-2-methylcyclohexanone

: 85114-34-7
Succinic acid mono-((1R,2S,4R)-4-tert-butyl-2-methyl-cyclohexyl) ester; compound with (S)-1-phenyl-ethylamine

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / lithium aluminum hydride / diethyl ether / 0.75 h / 0 °C

2: 150 g / pyridine / 2 h / Heating

3: ethyl acetate; methanol

With pyridine; lithium aluminium tetrahydride; In methanol; diethyl ether; ethyl acetate;
DOI:10.1021/ja00348a048