HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → α,α,3,5-Tetrafluorobenzeneacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 39058314 | HCID 39058314 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | α,α,3,5-Tetrafluorobenzeneacetic acid | HCID 22492123 | — |
Reaction Steps
A solution of ethyl 3,5-difluorophenyl-α,α-difluoroacetate (from Example D24 below; 1 molar eq.) in 50% aqueous ethanol was treated with lithium hydroxide (1.5 molar eq.). The solution was stirred for 3 hours at ambient temperature then concentrated via rotary evaporation. The residue was taken up in water; a small amount of 1 N NaOH was added to make basic. The aqueous mixture was extracted with ether. The aqueous layer was acidified to pH 3 with 1 N HCl. The acid was extracted thrice with methylene chloride. The combined methylene chloride extracts were dried over Na2SO4, filtered, and concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06861558B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-c596f46d38ba49fbb7c2a4e41635c4b8 |
| Source note | uspto-grants-2005_03 |