HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086454Generated: November 2, 2026
Acetonitrile → Ethyl 4,4,4-trifluoro-3-hydroxybutanoate
https://huagongshe.com/reaction/2086454
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | P-Cymene | HCID 7463 | — |
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Solvent | Triethylammonium formate | HCID 11084032 | — |
| Product | Ethyl 4,4,4-trifluoro-3-hydroxybutanoate | HCID 136210 | — |
Reaction Steps
To 10 mL of acetonitrile were added 5 mL of a mixture of formic acid-triethylamine (5:2 in molar ratio), 7 mg of RuCl[(1R,2R)-p-TsNHCH(C6H5)CH(C6H5)NH2] (p-cymene), and 1.0 g of ethyl 4,4,4-trifluoro-3-oxobutanoate, and the whole was stirred at 35° C. for 15 hours, followed by concentration under reduced pressure using an evaporator. To the resulting concentrate were added 10 mL of water and 10 mL of ethyl acetate, and then a saturated sodium carbonate aqueous solution was added thereto under stirring until the pH became 7 or higher. The ethyl acetate layer separated from the aqueous layer was concentrated to obtain optically active ethyl 4,4,4-trifluoro-3-hydroxybutanoate. Upon the measurement under the above conditions, the optical purity and conversion were found to be 95.0% e.e. and 99.9%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06723871B2 |
|---|
| Source dataset | uspto-grants-2004_04 |
|---|
| ORD ID | ord-7f40b0feb4fe4523a5609b0fb6dfb186 |
|---|
| Source note | uspto-grants-2004_04 |
|---|