Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | 3,4-Difluorobenzene-1,2-diamine | HCID 2736753 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178505459 | HCID 178505459 | 27.2% |
Reaction Steps
To a solution of 1,2-diamino-3,4-difluoro-benzene (996 mg, 6.9 mmol) in 20 mL of ethanol in a 25 mL microwave tube, are added 2.0 mL (33.3 mmol) of carbon disulfide. The tube is capped and the reaction mixture is heated under microwaves at 120° C. twice for 20 minutes, upon which 1.0 mL (16.6 mmol) of carbon disulfide is added and heating under microwaves is pursued for 20 minutes. Carbon disulfide 2.0 mL (33.3 mmol) is added and heating is pursued for 30 minutes under microwaves at 150° C. The reaction mixture is then cooled to room temperature and concentrated to dryness under reduced pressure. The residue is dissolved into ethyl acetate and concentrated to dryness under reduced pressure. The residue is triturated into diisopropylether, filtered and washed once with diisopropylether. The solid is dried under reduced pressure. 0.35 g of 6,7-difluoro-1H-benzimidazole-2-thiol is obtained as mauve solid. LCMS-DAD-ELSD: 185(−): [M−H]−; 186(+): [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08163768B2 |
|---|
| Source dataset | uspto-grants-2012_04 |
|---|
| ORD ID | ord-63d3590e7827453595b7fc93b1982c04 |
|---|
| Source note | uspto-grants-2012_04 |
|---|