HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrifluoroethylene → HCID 14405126, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrifluoroethylene | HCID 6594 | — |
| Reactant | 4-Methylcatechol | HCID 9958 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Sulfolane | HCID 31347 | — |
| Product | HCID 14405126 | HCID 14405126 | — |
Reaction Steps
124 g of 4-methylpyrocatechol were initially introduced into 300 ml of tetramethylene sulphone, together with 110 g of potassium hydroxide, at 110° C. 170 g of trifluorochloroethylene were then passed in in the course of 4 hours. The mixture was then distilled over a column under 15 mm Hg, the distillate being removed up to a transition temperature of 85° C. After separating off the aqueous phase in the receiver, the product was again distilled. 133 g ( 65% of theory) of 6-methyl-2,2,3-trifluoro-1,4-benzodioxene were obtained at a boiling point 70°-72° C./12 mm Hg (nD20 : 1.4565).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04438275 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-eb45545f58e249a789afd37932e59859 |
| Source note | uspto-grants-1984_03 |