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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-Acetoxy-2,2-dichloro-3,3,3-trifluoropropyl)-2,3-dichlorobenzeneHCID 19849816—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product(2-Chloro-3,3,3-trifluoropropen-1-yl)-2,3-dichlorobenzeneHCID 54504845—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868202
Source datasetuspto-grants-1989_09
ORD IDord-4212126600c34534939c0881d70c3edf
Source noteuspto-grants-1989_09