Trifluoroacetic acid → HCID 57983484, compound
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[C:10]([CH3:13])([CH3:12])[C:9](=[O:14])[C:8]([C:15]([NH:17][CH2:18][C:19]([O:21]C(C)(C)C)=[O:20])=[O:16])=[C:7]2[OH:26].C(O)(C(F)(F)F)=O>O>[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[C:10]([CH3:13])([CH3:12])[C:9](=[O:14])[C:8]([C:15]([NH:17][CH2:18][C:19]([OH:21])=[O:20])=[O:16])=[C:7]2[OH:26]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a flask containing 1,1-dimethylethyl N-((8-fluoro-4-hydroxy-1,1-dimethyl-2-oxo-naphthalen-3-yl)carbonyl)glycinate (1.5 g, 4.1 mmol) was added TFA (20 mL). The reaction was stirred under nitrogen for 1 hours and then concentrated in vacuo to afford an oil. Addition of water caused a white precipitate to form. The solid was collected by filtration, washed with water, washed with ether, and then dried in vacuo (0.68 g). MS (m/z)=308 (M+H)+. Calculated for C15H14FNO5 307.08.
Workup
- concentrationconcentrated in vacuo
- customto afford an oil
- customto form
- filtrationThe solid was collected by filtration
- washwashed with water
- washwashed with ether
- customdried in vacuo (0.68 g)
Sources & evidence
- ORD record
- ord-19b7e5ea1ea74ccba0323a855fa2b341
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07635715B2
Reaction notes
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