HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5,6-Dichloro-1-(methylsulphonyl)-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 5,6-Dichloro-1H-benzimidazole | HCID 331775 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,6-Dichloro-1-(methylsulphonyl)-benzimidazole | HCID 20313044 | — |
Reaction Steps
A solution of methanesulphonyl chloride (60 parts) in acetone (800 parts) was added dropwise to a suspension of 5,6-dichloro-benzimidazole (94 parts) in acetone (240 parts) containing triethylamine (50 parts). A precipitate of triethylamine hydrochloride was observed and the temperature rose to 40° C. The mixture was heated under reflux for 10 minutes and then stirred at room temperature for 20 hours. On pouring into cold water (4000 parts) a solid product precipitated out, which was filtered off, washed with water, dried and recrystallised from acetone (charcoal) to give 5,6-dichloro-1-(methylsulphonyl)-benzimidazole (61 parts) as pale yellow needles, melting point 191°-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04109004 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-4a8e25bb60ef4025aae0c947bbe4344a |
| Source note | uspto-grants-1978_08 |