HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium tert-butoxide → 1,2-Dichloro-3-(trifluoroprop-1-YN-1-YL)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | (2-Chloro-3,3,3-trifluoropropen-1-yl)-2,3-dichlorobenzene | HCID 54504845 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1,2-Dichloro-3-(trifluoroprop-1-YN-1-YL)benzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868202 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-c9c5eabdcb264a7281d296babd8fe870 |
| Source note | uspto-grants-1989_09 |