HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5-(3-chloropropyl)-1-(alpha-ethoxycarbonyl-p-cyanobenzyl)-1H-imidazole hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(alpha-ethoxycarbonyl-p-cyanobenzyl)-1H-imidazole-5-propanol | HCID 19930417 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(3-chloropropyl)-1-(alpha-ethoxycarbonyl-p-cyanobenzyl)-1H-imidazole hydrochloride | HCID 19930415 | — |
Reaction Steps
To a solution of 5.75 g of thionylchloride in 80 ml of methylene chloride is added 8.4 g of 1-(α-ethoxycarbonyl-p-cyanobenzyl)-1H-imidazole-5-propanol as a solid in portions. When addition is complete, the solution is refluxed for 1.5 h, cooled in ice and filtered to obtain 5-(3-chloropropyl)-1-(α-ethoxycarbonyl-p-cyanobenzyl)-1H-imidazole hydrochloride. The salt is partitioned between methylene chloride and saturated sodium bicarbonate. The organic extracts were washed with water, dried over sodium sulfate and evaporated to yield the free base.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04728645 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-8640afb8ef5546adbeea702db01b0bfa |
| Source note | uspto-grants-1988_03 |