HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975215Generated: October 30, 2026
Water → 1-(5-Bromothiophen-2-yl)-2,2,2-trifluoroethan-1-one
https://huagongshe.com/reaction/975215
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1-(5-Bromothiophen-2-yl)-2,2,2-trifluoroethanol | HCID 19971580 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(5-Bromothiophen-2-yl)-2,2,2-trifluoroethan-1-one | HCID 19971587 | — |
Reaction Steps
2.93 g (0.011 mol) of 2,2,2-trifluoro-1-(5-bromo-2-thienyl)ethanol and 0.19 g (0.0006 mol) of tetrabutylammonium hydrogen sulfate are dissolved in 100 ml of methylene chloride at room temperature. 6.9 ml (0.014 mol) of an approximately 12% strength sodium hyochlorite solution are metered in within 5 minutes with vigorous stirring and the mixture is stirred for a further 4 hours at room temperature. The reaction mixture is added to 100 ml of water, the phases are separated, the aqueous phase is extracted several times with methylene chloride and the combined organic phases are washed with saturated aqueous sodium chloride solution. After drying the organic phase with sodium sulfate, the volatiles are distilled off. Following distillation of the crude product in a kugelrohr (0.3 mbar, 40°-60° C. bath temperature), 0.48 g (39% of theory) of 5-bromo-2-trifluoroacetylthiophene. nD20 : 1.5309.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05608062 |
|---|
| Source dataset | uspto-grants-1997_03 |
|---|
| ORD ID | ord-a14f8ecb6f7a40bb92f007a077454e5e |
|---|
| Source note | uspto-grants-1997_03 |
|---|