HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77024Generated: October 29, 2026
Ethyl alpha-oxo-4-(trifluoromethyl)benzeneacetate → Hydroxy 4-(trifluoromethyl)phenylacetic acid ethyl ester
https://huagongshe.com/reaction/77024
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl alpha-oxo-4-(trifluoromethyl)benzeneacetate | HCID 2774410 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Hydroxy 4-(trifluoromethyl)phenylacetic acid ethyl ester | HCID 20286794 | 87.3% |
Reaction Steps
Ethyl 2-oxo-2-(4-(trifluoromethyl)phenyl)acetate (500 mg, 2.03 mmol) is dissolved in absolute EtOH (10 mL) and cooled at 0° C. under N2. NaBH4 (38.4 mg, 1.02 mmol) is added in two portions and the resulting suspension is allowed to warm to RT and stirred for 45 minutes. The solvent is evaporated, the resulting residue is diluted with Et2O and cool water is added. The organic layer is separated, washed with water and brine, dried over Na2SO4, filtered and evaporated obtaining intermediate I149 as a colorless oil (440 mg, 87% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835682B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-43254763d3064c23884c9cb44e62cf07 |
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| Source note | uspto-grants-2014_09 |
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