HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 131711667, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 19890747 | HCID 19890747 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 131711667 | HCID 131711667 | 74.4% |
Reaction Steps
A mixture of 1.9 parts of 5-[4-(diphenylmethyl)-1-piperazinylmethyl]-1-methyl-1H-benzimidazole-2-methanol, 1.55 parts of acetic acid anhydride and 45 parts of methylbenzene is stirred and refluxed for 2 hours. The reaction mixture is cooled, washed with a diluted ammonium hydroxide solution and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is crystallized from a mixture of methylbenzene and 2,2'-oxybispropane (20:20 by volume). The product is filtered off and dried, yielding 1.5 parts (74.4%) of {5-[4-(diphenylmethyl)-1-piperazinylmethyl]-1-methyl-1H-benzimidazol-2-ylmethyl}acetate; mp. 201.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04179505 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-7b537ddc0ecf45fcae9726bd775bf79c |
| Source note | uspto-grants-1979_12 |