HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 178480057, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 54334135 | HCID 54334135 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178480057 | HCID 178480057 | 47.1% |
Reaction Steps
A mixture of 5-[[3,5-bis(1,1-dimethylethyl)-4hydroxyphenyl]methylene]-1,5-dihydro-l-methyl-2-(methylthio)-4H-imidazol-4-one (3.0 g, 8 mmoles), guanidine hydrochloride (1.7 g, 18 mmoles) and 50 mL of ethanol is treated with potassium t-butoxide (1.5 g, 13 mmoles) and heated under reflux for 20 hours, then stirred into 400 mL of water. The precipitate is filtered off, rinsed with water, dried, and recrystallized from acetone to afford the product (1.4 g), mp 286°-287° C. (dec). A sample recrystallized from DMF/EtOH was analytically pure which is N-[5-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-4,5-dihydro-1-methyl-4-oxo-1H-imidazol-2-yl]guanidine, mp 288°-290° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05494927 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-283405f4d6504491b0b0b9e79fc7a9bf |
| Source note | uspto-grants-1996_02 |