HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Trifluoromethyl 1-chloro-N-(p-chlorobenzyl)thioformimidate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methanesulfenyl chloride, trifluoro- | HCID 67900 | — |
| Reactant | 1-Chloro-4-(isocyanomethyl)benzene | HCID 2757409 | — |
| Product | Trifluoromethyl 1-chloro-N-(p-chlorobenzyl)thioformimidate | HCID 18930385 | 68% |
Reaction Steps
Trifluoromethylsulfenyl chloride (4.0 g, 0.03 mol) is bubbled over 30 minutes into a solution of 4-chlorobenzylisonitrile (3.0 g, 0.02 mol) in methylene chloride, causing the formation of a white precipitate. The suspension is stirred for 16 hours at room temperature and filtered to remove solids. The white filter cake is washed with methylene chloride and solvent is removed under reduced pressure to obtain an amber oil. Bulb-to-bulb distillation of the oil (90°-100° C., 0.05 mmhg) gives the title product as a colorless oil (3.9 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05306827 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-b2e43a961f6743d3b28e2d4174581de4 |
| Source note | uspto-grants-1994_04 |