HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethyl 4,4,5,5-tetrafluoro-3-hydroxy-pentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 4,4,5,5-tetrafluoro-3-oxo-pentanoate | HCID 13356428 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 4,4,5,5-tetrafluoro-3-hydroxy-pentanoate | HCID 86691164 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Ethyl 4,4,5,5-tetrafluoro-3-oxo-pentanoate (25.7 g, 0.119 mol) was dissolved in toluene (260 ml) and cooled to 0° C. Sodium borohydride (5.4 g, 0.143 mol) was added portionwise, and the mixture was allowed to reach room temperature overnight with stirring. The mixture was then cooled to 0° C. and acidified with 1M HCl. The phases were separated, the aqueous phase was extracted two times with ethyl acetate, the combined organic phases were dried over magnesium sulfate and the solvent was reduced under reduced pressure. The residue was dissolved in a minimum amount of methanol and evaporated to dryness under reduced pressure to yield 22.9 g (0.105 mol, 88%) that were used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877934B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-6c11e16691494cbc8fd8f84292e0e77b |
| Source note | uspto-grants-2014_11 |