HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2,2,2-trichloroacetimidate → 2-(2-Trichloromethyl-1H-benzoimidazole-5-sulfonyl)-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2,2,2-trichloroacetimidate | HCID 100479 | — |
| Reactant | 3,4-Diamino-benzene-sulfonylethan-2-ol | HCID 15596955 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2-Trichloromethyl-1H-benzoimidazole-5-sulfonyl)-ethanol | HCID 178527414 | — |
Reaction Steps
500 mg (2.31 mmol) 3,4-diamino-benzene-sulfonylethan-2-ol were dissolved in 10 mL concentrated acetic acid. 0.4 mL (1.4 equiv.) methyl-2,2,2-trichloroacetimidate were added slowly and the resulting mixture was stirred at room temperature for 4 h. The mixture was diluted with 100 mL toluene and the solvent was removed under reduced pressure. The residue was rinsed with toluene, filtered and dried under vacuo to give a brown crystalline solid pure enough for all further reactions. Yield: 680 mg MS (ES+): m/e=345, chloro pattern.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741341B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-defa08f4eaed4ef6b84a8a36d7d5959a |
| Source note | uspto-grants-2010_06 |