Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607910Generated: October 29, 2026

Potassium tert-butoxide → 1,2-Dichloro-3-(trifluoroprop-1-YN-1-YL)benzene

https://huagongshe.com/reaction/1607910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant(2-Chloro-3,3,3-trifluoropropen-1-yl)-2,3-dichlorobenzeneHCID 54504845—
Solventtert-ButanolHCID 6386—
Product1,2-Dichloro-3-(trifluoroprop-1-YN-1-YL)benzeneHCID 19849819—

Reaction Steps

To a solution of 31.7 g of (2-chloro-3,3,3-trifluoropropen-1-yl)-2,3-dichlorobenzene in 50 ml of tert-butanol, there is added dropwise at RT a solution of 14.1 g of potassium tert-butylate in 750 ml of tert-butanol in such a manner that the temperature of the reaction solution does not exceed 30° C. After continued stirring at RT for 18 h, the mixture is taken up in ice-water and extracted with ether. The organic phases are combined, washed with water and sodium chloride solution, and concentrated by evaporation. There is thus obtained, after distillation in vacuo, 2,3-dichloro-(3,3,3-trifluoropropyn-1-yl)-benzene in the form of colourless oil, b.p. 92°-98° C. at 22 mb (compound No. 2.27).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868202
Source datasetuspto-grants-1989_09
ORD IDord-c9c5eabdcb264a7281d296babd8fe870
Source noteuspto-grants-1989_09