HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607909Generated: November 3, 2026
(1-Acetoxy-2,2-dichloro-3,3,3-trifluoropropyl)-2,3-dichlorobenzene → (2-Chloro-3,3,3-trifluoropropen-1-yl)-2,3-dichlorobenzene
https://huagongshe.com/reaction/1607909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (1-Acetoxy-2,2-dichloro-3,3,3-trifluoropropyl)-2,3-dichlorobenzene | HCID 19849816 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (2-Chloro-3,3,3-trifluoropropen-1-yl)-2,3-dichlorobenzene | HCID 54504845 | — |
Reaction Steps
A solution of 59.0 g of (1-acetoxy-2,2-dichloro-3,3,3-trifluoropropyl)-2,3-dichlorobenzene in 350 ml of acetic acid is heated to 40° C., and 13.0 g of zinc powder are added portionwise. To effect completion of the reaction, the reaction mixture is heated at 90° C. for 3 hours. In further processing, thereaction mixture is taken up in ice-water, and extracted with ether. The combined organic phases are washed with water, sodium hydrogen carbonate solution and sodium chloride solution; they are then dried over magnesium sulfate, and concentrated by evaporation to thus obtain (2-chloro-3,3,3-trifluoropropen-1-yl)-2,3-dichlorobenzene in the form of yellow oil (compound No. 4.10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04868202 |
|---|
| Source dataset | uspto-grants-1989_09 |
|---|
| ORD ID | ord-4212126600c34534939c0881d70c3edf |
|---|
| Source note | uspto-grants-1989_09 |
|---|