HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethyl 4,4-difluoro-3-hydroxy-pentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4,4-Difluoro-3-oxopentanoic acid ethyl ester | HCID 86221379 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 4,4-difluoro-3-hydroxy-pentanoate | HCID 89825740 | 70,588.203% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Ethyl 4,4-difluoro-3-oxo-pentanoate (12.4 g, 0.068 mmol) was dissolved in toluene (100 ml) and cooled to 0° C. Sodium borohydride (3.12 g, 0.083 g) 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 1 m 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 removed under reduced pressure. The residue was dissolved in a minimum amount of methanol, the resulting solution was evaporated to dryness under reduced pressure to yield 8.76 g of a residue (0.048 mol, 70%) that were used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321724B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-9e24c043b2c5460caed0ccfd8af942ab |
| Source note | uspto-grants-2016_04 |