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Water → Methyl 2-(4-fluoro-3-nitrophenyl)-4-hydroxy-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate

HRID 2045571
Notes
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Reaction equation

HRID 2045571 reaction equation
[F:1][C:2]1[CH:19]=[CH:18][C:5](/[CH:6]=[N:7]/[C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=2)=[CH:4][C:3]=1[N+:20]([O-:22])=[O:21].[CH:23](=[O:27])[CH:24]([CH3:26])[CH3:25].O>O1CCCC1.FC(F)(F)S([O-])(=O)=O.[Y+3].FC(F)(F)S([O-])(=O)=O.FC(F)(F)S([O-])(=O)=O>[F:1][C:2]1[CH:19]=[CH:18][C:5]([CH:6]2[C:24]([CH3:26])([CH3:25])[CH:23]([OH:27])[C:17]3[C:8](=[CH:9][CH:10]=[C:11]([C:12]([O:14][CH3:15])=[O:13])[CH:16]=3)[NH:7]2)=[CH:4][C:3]=1[N+:20]([O-:22])=[O:21]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 962WaterHCID 6561IsobutyraldehydeHCID 178498131HCID 178498131, compound

Product 1

HCID 67442290Methyl 2-(4-fluoro-3-nitrophenyl)-4-hydroxy-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylateYield 70.1%

Reagents, catalysts & solvents 2

HCID 2733939Yttrium trifluoromethanesulfonate
Catalyst
HCID 8028TetrahydrofuranSolvent

Procedure

To a suspension of (E)-methyl 4-(4-fluoro-3-nitrobenzylideneamino)benzoate (3.62 g, 12.0 mmol) in tetrahydrofuran (24 mL), yttrium(III) trifluoromethanesulfonate (75 mg, 0.12 mmol) and isobutyraldehyde (0.87 g, 12.0 mmol) were added under nitrogen at room temperature The resultant mixture was stirred at room temperature for 20 hours (turned into clear in 10 min). Water was added to the reaction mixture and extracted with Ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous sodium sulfate. Solvent was removed and the residue was purified by column (petroleum ether/ethyl acetate=3:1, silica gel) to afford methyl 2-(4-fluoro-3-nitrophenyl)-4-hydroxy-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate 3.15 g (70%) as a yellow solid.

Workup

  1. extractionextracted with Ethyl acetate
  2. washThe combined organic layers were washed with brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. customSolvent was removed
  5. customthe residue was purified by column (petroleum ether/ethyl acetate=3:1, silica gel)

Sources & evidence

ORD record
ord-071d6a8710c4449f9564d352ba064524
Source dataset
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08586747B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes