Trifluoroacetic acid → HCID 68500250, compound
Reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[CH:14]=[C:13]([S:15]([CH3:18])(=[O:17])=[O:16])[CH:12]=[C:11]([C:19]([O:21]C(C)(C)C)=[O:20])[CH:10]=1.FC(F)(F)C(O)=O>ClCCl>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[CH:14]=[C:13]([S:15]([CH3:18])(=[O:16])=[O:17])[CH:12]=[C:11]([C:19]([OH:21])=[O:20])[CH:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of tert-butyl 2′,4′-difluoro-5-(methylsulfonyl)biphenyl-3-carboxylate (77 mg, 0.21 mmol) in dichloromethane (1.05 mL) was added trifluoroacetic acid (1.05 mL). The mixture was stirred at ambient temperature for 30 min. The mixture was concentrated to dryness to give the title compound.
Workup
- concentrationThe mixture was concentrated to dryness
Sources & evidence
- ORD record
- ord-815dde1b6b48479999f26cab808991f8
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08247401B2
Reaction notes
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