HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloromethanethiol → 6-chloro-2-ethyl-1-trichloromethanesulfenyl-1H-imidazo[4,5-b]quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloromethanethiol | HCID 6390 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-chloro-2-ethyl-1H-imidazo[4,5-b]quinoxaline | HCID 178437541 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-chloro-2-ethyl-1-trichloromethanesulfenyl-1H-imidazo[4,5-b]quinoxaline | HCID 21436001 | — |
Reaction Steps
Two parts of 6-chloro-2-ethyl-1H-imidazo[4,5-b]quinoxaline was combined with two parts of perchloromethyl mercaptan in sixty parts of tetrahydrofuran. One part of triethylamine was added slowly dropwise at 30° over a one-hour period. The mixture was poured into water and crude product was collected. The material was recrystallized from a chloroform:hexane mixture to give 1 part of 6-chloro-2-ethyl-1-trichloromethanesulfenyl-1H-imidazo[4,5-b]quinoxaline, m.p. 250° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04022777 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-a7b499623615418e9d6c65c4a43e77e0 |
| Source note | uspto-grants-1977_05 |