HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Diaminobenzonitrile → 2-(Chloromethyl)-1H-benzo[d]imidazole-6-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Diaminobenzonitrile | HCID 737285 | — |
| Reactant | Ethyl 2-chloroethanecarboximidate hydrochloride | HCID 12470659 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Chloromethyl)-1H-benzo[d]imidazole-6-carbonitrile | HCID 21844453 | 54.9% |
Reaction Steps
3.42 g of 3,4-diaminobenzonitrile and 4.06 g of ethyl chloroacetoimidate hydrochloride were dissolved in 100 ml of ethanol, and the solution was refluxed under heating for 3 hours. After cooling and distilling off the solvent, the resulting residue was dissolved in ethyl acetate, washed with water, and then dried. After distilling off the solvent, the crystals thus precipitated were collected by filtration to obtain 2.7 g of 2-chloromethyl-5-benzimidazolecarbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576343 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-9f0d54ad97a44a509a1348fd91dfa50f |
| Source note | uspto-grants-1996_11 |