HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 67002033, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Methanol | HCID 887 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Product | HCID 67002033 | HCID 67002033 | — |
Reaction Steps
As shown in Method E, imidazole 10 (R8 =CH3) is treated with any ether cleaving reagent such as 48% HBr in acetic acid, pyridine-HCl, AlCl3 /C6H6, and BBr3 /CH2Cl2 at 0° to the reflux temperature of the solvent for about 1-24 hours to obtain imidazole phenol 11 (X=CH2). Imidazole 10 (R8 =CH2C6H5) is treated with a suitable solvent such as an alcohol (CH3OH, EtOH, and the like) or acetic acid at ambient temperature for a period of about 15 minutes to about 15 hours in the presence of a suitable catalyst such as 10% Pd on carbon, platinum oxide, and the like, at a pressure of up to about 60 psi to afford imidazole 11 (X=CH2 or X=O when m and n are >1). ##STR16##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04602093 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-03fe9124cfd34e25b3f830a29241163f |
| Source note | uspto-grants-1986_07 |