HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Chloro[2-(2,4,6-trichlorophenyl)hydrazinylidene]acetyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Chloro-2-[2-(2,4,6-trichlorophenyl)hydrazinylidene]acetic acid | HCID 85793633 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Chloro[2-(2,4,6-trichlorophenyl)hydrazinylidene]acetyl chloride | HCID 71365096 | — |
Reaction Steps
A mixture consisting of 61 g. (0.20 mole) chloroglyoxylic acid (2,4,6-trichlorophenyl)hydrazone, 200 ml. carbon tetrachloride, and 100 ml. thionyl chloride was heated at the reflux temperature for 6 1/2 hrs. The carbon tetrachloride and thionyl chloride were removed by evaporation under reduced pressure and 50° C. to give 64 g. of an oil. The oil was extracted with technical hexane and the insoluble starting material was removed by filtration. The technical hexane was removed by evaporation under reduced pressure to give chloroglyoxyloyl chloride (2,4,6-trichlorophenyl) hydrazone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006132 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-ff31609494244da689df6cb9df14335d |
| Source note | uspto-grants-1977_02 |