HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 14722476, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(4-Nitrobenzyl)-2-hydroxymethylbenzimidazole | HCID 14722475 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 14722476 | HCID 14722476 | — |
Reaction Steps
To a solution of 2.2 g 1-(4-nitrobenzyl)-2-hydroxymethylbenzimidazole in 30 mL of chloroform was added 3.3 mL of thionyl chloride. The reaction mixture was stirred at room temperature for 18 hours and then concentrated in vacuo. The residue was taken up in water, neutralized with K2CO3 to a pH of 10 and extracted into methylene chloride. The organic layer was dried over Na2SO4 and concentrated to give 2 g of 1-(4-nitrobenzyl)-2-chloromethylbenzimidazole as a yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04880804 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-d06229224082413db601a69d10cbacb4 |
| Source note | uspto-grants-1989_11 |