HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 20261653, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 13600722 | HCID 13600722 | — |
| Reactant | HCID 20261709 | HCID 20261709 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20261653 | HCID 20261653 | — |
Reaction Steps
5-Chloromethyl-2-dimethylaminomethylbenzimidazole, 2hydrochloride (melting point 248.4° C., 3.64 g) was produced by subjecting 2-dimethylaminomethyl-5-hydroxymethylbenzimidazole (3 g) and thionylchloride (10.5 ml) to a 4-hour refluxing with heat. 2-Mercaptopropionitrile (1.05 g) was changed into sodium salt by sodium ethoxide and, at a temperature of 0° C., methanol solution of the above-mentioned chloromethyl compound was added gradually and the mixture was stirred through one whole night at the room temperature to yield 5-[(2-cyanoethyl)thiomethyl]-2-dimethylaminomethylbenzimidazole (3.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04550118 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-0f2febcda39844b08827069bbb96b160 |
| Source note | uspto-grants-1985_10 |