HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → 1-Ethoxycarbonylmethyl-3-phenyl-benzimidazolium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 1-Phenyl-1H-benzoimidazole | HCID 606669 | — |
| Product | 1-Ethoxycarbonylmethyl-3-phenyl-benzimidazolium bromide | HCID 14067551 | 56% |
Reaction Steps
Using the procedure of Step B of Example 1, 1-phenylbenzimidazole [prepared from N-phenyl-o-phenylenediamine with 4HCl and formic acid] and ethyl bromoacetate were reacted to obtain a 56% of 1-ethoxycarbonylmethyl-3-phenyl-benzimidazolium bromide which after crystallization from a mixture of ethyl acetate and methanol melted at 180°-181° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04151280 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-884eb9d0373d47e7aacf2db69e72e913 |
| Source note | uspto-grants-1979_04 |