HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-chloro-4-[chloro(4-chlorophenyl)methyl]phenyl-1,2,4-triazine-3,5(2H,4H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(3-Chloro-4-((4-chlorophenyl)hydroxymethyl)phenyl)-1,2,4-triazine-3,5(2H,4H)-dione | HCID 135108 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-chloro-4-[chloro(4-chlorophenyl)methyl]phenyl-1,2,4-triazine-3,5(2H,4H)-dione | HCID 22557357 | 83.1% |
Reaction Steps
To a stirred mixture of 16 parts of 2-[3-chloro-4-[(4-chlorophenyl)hydroxymethyl]phenyl]-1,2,4-triazine-3,5(2H,4H)-dione and 150 parts of trichloromethane were added dropwise, during a period of 5 minutes, 16 parts of thionyl chloride. Upon completion, stirring was continued for 3 hours at reflux temperature. The reaction mixture was evaporated in vacuo. Methylbenzene was added and the whole was evaporated again, yielding 14 parts (83.1%) of 2-[3-chloro-4-[chloro(4-chlorophenyl)methyl]phenyl]-1,2,4-triazine-3,5(2H,4H)-dione as a residue (intermediate 107).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04778887 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-8e71594f8d414768a6b8db52cfc0e7d1 |
| Source note | uspto-grants-1988_10 |