Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | HCID 14305254 | HCID 14305254 | — |
| Product | HCID 14305256 | HCID 14305256 | 28.8% |
Reaction Steps
A mixture of 7 parts of 1-[phenyl(2-pyridinyl)methyl]-1H-imidazole-5-carboxylic acid, 5.5 parts of concentrated sulfuric acid and 140 parts of cyclohexanol was stirred for 2 days at 100° C. The reaction mixture was evaporated (at an oil pump) and the residue was taken up in dichloromethane. The organic layer was washed with a sodium hydroxide solution, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried in vacuo at 60° C., yielding 2.6 parts (28.8%) of cyclohexyl 1-[phenyl(2-pyridinyl)methyl]-1H-imidazole-5-carboxylate; mp. 161.0° C. (compound 1.255).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04770689 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-35bc88c801724dcebcdce623da0507d3 |
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| Source note | uspto-grants-1988_09 |
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