HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066929Generated: November 3, 2026
Ethyl Acetate → 2-Hydroxy-4-phenyl-2-trifluoromethyl-valeric acid ethyl ester
https://huagongshe.com/reaction/1066929
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 2-Oxo-4-phenylvaleric acid ethyl ester | HCID 17935637 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Hydroxy-4-phenyl-2-trifluoromethyl-valeric acid ethyl ester | HCID 17935608 | — |
Reaction Steps
4.4 g of 2-oxo-4-phenylvaleric acid ethyl ester is dissolved in 40 ml of tetrahydrofuran and mixed at −78° C. with 3.6 ml of trifluoromethyl-trimethylsilane and 2 ml of 1 M tetrabutylammonium fluoride in tetrahydrofuran. After 24 hours at −78° C., another 20 ml of 1 M tetrabutylammonium fluoride in tetrahydrofuran is added. It is stirred for 1.5 hours at 0° C., ethyl acetate and saturated common salt solution are added, the organic phase is separated, and it is washed with saturated common salt solution and water. Then, it is dried (Na2SO4) and concentrated by evaporation and distilled on a bulb tube. 4.4 g of 2-hydroxy-4-phenyl-2-trifluoromethyl-valeric acid ethyl ester, boiling point 95-100° C./0.04 hPa, is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06245804B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-3fb275e43aa146e1822d3b4a35a587fc |
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| Source note | uspto-grants-2001_06 |
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