HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one | HCID 3017358 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one | HCID 20385630 | — |
Reaction Steps
A mixture of 20 parts of 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one, 34 parts of sulfinyl chloride and 300 parts of trichloromethane is stirred and refluxed for 4 hours. The trichloromethane is evaporated and the residue is crystallized from 4-methyl-2-pentanone (activated charcoal). The product is filtered off (the filtrate is set aside), yielding a first fraction of 8.2 parts of 5-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one. The filtrate, which was set aside, is concentrated and the concentrate is stirred with 2,2'-oxybispropane. The precipitated product is filtered off and dried, yielding a second fraction of 8 parts of 5-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04066772 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-6633218ba4494898a80e47d25064d2d0 |
| Source note | uspto-grants-1978_01 |