Hydrochloric Acid → HCID 15029627, compound
Reaction equation
Cl.[F:2][C:3]1[CH:12]=[C:11]([F:13])[CH:10]=[C:9]2[C:4]=1[C:5](=[O:19])[CH:6]=[C:7]([O:15][CH:16](C)C)[C:8]2=[O:14]>CO>[F:2][C:3]1[CH:12]=[C:11]([F:13])[CH:10]=[C:9]2[C:4]=1[C:5](=[O:19])[CH:6]=[C:7]([O:15][CH3:16])[C:8]2=[O:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 0.48 g (13.2 mM) of anhydrous hydrogen chloride in 15 mL of methanol was treated with 0.175 g (0.694 mM) of 5,7-difluoro-2-isopropoxy-1,4-naphthoquinone. The mixture was heated to solvent reflux temperature for 0.33 hours, cooled to room temperature and concentrated in vacuo to give 0.13 g of product. 1H NMR (dmso-d6): δ=7.8 (m, 1H), 7.68 (dd, 1H, JH-Fortho =7.5 Hz), 6.31 (s, 1H), 3.86(s, 3H).
Workup
- temperatureThe mixture was heated to solvent
- temperaturereflux temperature for 0.33 hours
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-3afd57460c4843eb9dcd62b9f239d302
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05541319
Reaction notes
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