HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245387Generated: October 31, 2026
Phenyl thioxochloroformate → 4-[1-(2,3-dichlorophenyl)ethyl]-1,3-dihydroimidazole-2-thione
https://huagongshe.com/reaction/2245387
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl thioxochloroformate | HCID 70498 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178437188 | HCID 178437188 | — |
| Reactant | HCID 178437189 | HCID 178437189 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[1-(2,3-dichlorophenyl)ethyl]-1,3-dihydroimidazole-2-thione | HCID 11601506 | — |
Reaction Steps
A 1:1 mixture of 4-[1-(2,3-dichloro-phenyl)-ethyl]-1H-imidazole (Intermediate A4), and 4-[1-(2,3-dichloro-phenyl)-vinyl]-1H-imidazole (Intermediate A3) (0.77 g, 3.2 mmol) in tetrahydrofuran (THF) (10 mL) and water (10 mL) was treated with NaHCO3 (1.64 g, 19.5 mmol) at rt for 10 m. Phenyl chlorothionoformate (1.1 mL, 7.95 mmol) was added and stirring was continued for 5 h. The mixture was diluted with water and extracted with hexane:ethyl acetate (3×). The organic portions were combined, dried over MgSO4, filtered and the solvent was removed under vacuum. The residue was dissolved in MeOH (20 mL) and treated with triethylamine (NEt3) (1 mL) for 18 h at rt. The mixture was concentrated onto silica gel. The material was purified by elution from silica gel with 1 to 2% MeOH: CH2Cl2. The solids were titurated with CHCl3: hexanes and collected on a glass frit to give a white solid 4-[1-(2,3-dichloro-phenyl)-ethyl]-1,3-dihydro-imidazole-2-thione (Compound 1) 40 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07683089B1 |
|---|
| Source dataset | uspto-grants-2010_03 |
|---|
| ORD ID | ord-8be801dd1b834abda28772732c215a44 |
|---|
| Source note | uspto-grants-2010_03 |
|---|