HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4,4,4-trifluoro-3-hydroxybutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4,4,4-trifluoro-3-hydroxybutanoate | HCID 136210 | — |
Reaction Steps
To a suspension of 91.2 g (2.4 mol) of sodium borohydride in 6 l of CH2Cl2 cooled at +2° C., are dropwise added 1473 g of ethyl 4,4,4-trifluoroacetoacetate while keeping temperature between +4° and +7° C. After the introduction, 100 ml of absolute ethanol are added while keeping temperature at +3° C. The reaction medium is washed with bicarbonated water. The organic phase is concentrated and the product is distilled at 78° C. under 10 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05036091 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-9e743ca4004c454e87fcc012cc0bc092 |
| Source note | uspto-grants-1991_07 |