HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537863Generated: October 25, 2026
Hexachloroethane → 2-Chloro-5-(4-(trifluoromethyl)phenyl)oxazole
https://huagongshe.com/reaction/537863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexachloroethane | HCID 6214 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 5-(4-(Trifluoromethyl)phenyl)oxazole | HCID 13268414 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-5-(4-(trifluoromethyl)phenyl)oxazole | HCID 71060395 | 97% |
Reaction Steps
LiHMDS (1.06 M in THF, 28.59 mL, 30.3 mmol) was added to a solution of 5-(4-(trifluoromethyl)phenyl)oxazole 30 (5.38 g, 25.25 mmol) in THF (100 mL) at −78° C., and the mixture was stirred at −78° C. for 1 h. A solution of hexachloroethane (8.96 g, 37.87 mmol) in THF (10 mL) was added at −78° C., and the mixture was stirred at −78° C. for 2 h and allowed to warm to room temperature and stirred for 14 h. The reaction was quenched by adding EtOAC: H2O (50 mL: 15 mL), and then extracted with Ethyl acetate. The extracts were washed with brine, dried (Na2SO4) and concentrated. The product was purified by column chromatography (Acetone/hexane as an eluent) to provide 2-chloro-5-(4-(trifluoromethyl)phenyl)oxazole 31 (6.05 g, 97% yield) as white solid. MS (ES) m/z 248 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08865709B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-09bbb1fa46e34782b40527a1e99e9334 |
|---|
| Source note | uspto-grants-2014_10 |
|---|