Hydrochloric Acid → HCID 86716098, compound
Reaction equation
[F:1][C:2]([F:22])([F:21])[O:3][C:4]1[CH:9]=[CH:8][C:7]([CH:10]([C:16]([O:18]CC)=[O:17])[C:11]([O:13]CC)=[O:12])=[CH:6][CH:5]=1.[OH-].[Na+].Cl>>[F:1][C:2]([F:21])([F:22])[O:3][C:4]1[CH:9]=[CH:8][C:7]([CH:10]([C:16]([OH:18])=[O:17])[C:11]([OH:13])=[O:12])=[CH:6][CH:5]=1Participants
4
Procedure
A mixture of diethyl 2-(4-(trifluoromethoxy)phenyl)malonate (5.6 g, 17.486 mmol, Intermediate 13: step a) and an aqueous 3 M NaOH solution was stirred in a 100° C. oil bath for 1 hour, cooled to room temperature, poured into ice water and acidified with 6 N aqueous HCl. The aqueous mixture was extracted with EtOAc. The EtOAc extract was dried over Na2SO4, filtered, and evaporated in vacuo to provide the title compound.
Workup
- extractionThe aqueous mixture was extracted with EtOAc
- extractionThe EtOAc extract
- dry with materialwas dried over Na2SO4
- filtrationfiltered
- customevaporated in vacuo
Sources & evidence
- ORD record
- ord-da73dfc6ef9646efafa568b87a2c474a
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09403816B2
Reaction notes
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