HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46381Generated: October 29, 2026
Boron tribromide → 1-(2-Hydroxy-5-(trifluoromethyl)phenyl)ethan-1-one
https://huagongshe.com/reaction/46381
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 1-(2-Methoxy-5-trifluoromethylphenyl)ethanone | HCID 9942601 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Hydroxy-5-(trifluoromethyl)phenyl)ethan-1-one | HCID 11769599 | 35.2% |
Reaction Steps
To a stirred solution of 1-[2-methoxy-5-(trifluoromethyl)phenyl]ethanone (35 g, 0.160 mol) in dry dichloromethane (400 mL) at 0° C. was added solid tetrabutylammonium iodide (2.96 g, 0.008 mol) followed by boron tribromide (33.96 mL, 0.353 mol) dropwise. After addition, the reaction mixture was stirred at room temperature for 90 minutes. The reaction mixture was cooled to 0° C. and quenched with ice. The mixture was extracted with diethyl ether (1000 mL). The organic layer was washed with water (2000 mL) and then saturated aqueous sodium chloride (1000 mL). After concentration of the organic layer at room temperature in vacuo, the crude product was purified by column chromatography (100-200 silica gel, 2% v/v diethyl ether in hexane) to give 11.5 g (35%) of the title compound as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08541588B2 |
|---|
| Source dataset | uspto-grants-2013_09 |
|---|
| ORD ID | ord-70b6a9696d13437a87ea73275552b049 |
|---|
| Source note | uspto-grants-2013_09 |
|---|