HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → (4-bromophenyl)(1H-imidazol-2-yl)phenylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | alpha-(p-Bromophenyl)-alpha-phenyl-1-(toluene-p-sulphonyl)imidazole-2-methanol | HCID 11838798 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-bromophenyl)(1H-imidazol-2-yl)phenylmethanol | HCID 12433864 | — |
Reaction Steps
A mixture of 24.8 g. (0.052 mol) of α-(p-bromophenyl)-α-phenyl-1-(toluene-p-sulphonyl)imidazole-2-methanol, 160 ml. of 2 N hydrochloric acid solution (0.156 mol) and about 500 ml. of water was boiled under reflux for 5 hours. After cooling the mixture was made alkaline by addition of ammonia. The precipitated solid was collected, treated with activated carbon in boiling toluene and crystallised from toluene. Melting point of the product was 156°-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04152441 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-26d17c2475ad44a4a697a698d7e18002 |
| Source note | uspto-grants-1979_05 |