Imidazole-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

Base Information

Chemical Name:Imidazole-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
CAS No.:245674-30-0
Molecular Formula:C₂₀H₂₆N₂O₂
Molecular Weight:326.439
Hs Code.:

Synonyms:Imidazole-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

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Chemical Property of Imidazole-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

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Technology Process of Imidazole-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

There total 8 articles about Imidazole-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester 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: 98.0%

: 65253-04-5
(-)-8-phenylmenthol

: 530-62-1
1,1'-carbonyldiimidazole

: 245674-30-0
Imidazole-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

Guidance literature:: In dichloromethane; at 20 ℃;
DOI:10.1016/S0040-4039(99)01638-X

Reference yield:

: 245674-48-0
2,3-Dihydro-pyrrole-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

: 245674-30-0
Imidazole-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: Et₃N / cyclohexane / 40 °C

2: 63 percent / Zn-Cu; NH₄Cl / methanol / 20 °C

3: 62 percent / m-CPBA; NaHCO₃ / CH₂Cl₂ / 0 °C

4: HCl; water / Heating

5: 98 percent / CH₂Cl₂ / 20 °C

With hydrogenchloride; water; copper; sodium hydrogencarbonate; ammonium chloride; triethylamine; 3-chloro-benzenecarboperoxoic acid; zinc; In methanol; dichloromethane; cyclohexane; 1: Cycloaddition / 2: Reduction / 3: Oxidation / 4: Decarboxylation / 5: Esterification;
DOI:10.1016/S0040-4039(99)01638-X

Reference yield:

: 245674-44-6
2-Hydroxy-pyrrolidine-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

: 245674-30-0
Imidazole-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 2,6-lutidine

2: 0.33 h / Heating

3: Et₃N / cyclohexane / 40 °C

4: 63 percent / Zn-Cu; NH₄Cl / methanol / 20 °C

5: 62 percent / m-CPBA; NaHCO₃ / CH₂Cl₂ / 0 °C

6: HCl; water / Heating

7: 98 percent / CH₂Cl₂ / 20 °C

With 2,6-dimethylpyridine; hydrogenchloride; water; copper; sodium hydrogencarbonate; ammonium chloride; triethylamine; 3-chloro-benzenecarboperoxoic acid; zinc; In methanol; dichloromethane; cyclohexane; 1: Esterification / 2: Elimination / 3: Cycloaddition / 4: Reduction / 5: Oxidation / 6: Decarboxylation / 7: Esterification;
DOI:10.1016/S0040-4039(99)01638-X