Cyclohexanecarboxaldehyde → HCID 66771669, compound
Reaction equation
C[O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7]([NH2:10])=[C:6]([OH:11])[CH:5]=1.[CH:13]1([CH:19]=O)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.C([O-])(=O)C.[Pb+4].C([O-])(=O)C.C([O-])(=O)C.C([O-])(=O)C>CO>[CH:13]1([C:19]2[O:11][C:6]3[CH:5]=[C:4]([C:3]([OH:2])=[O:12])[CH:9]=[CH:8][C:7]=3[N:10]=2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 4-amino-3-hydroxy-benzoic acid methyl ester (5 g, 29.91 mmol) in CH3OH (150 mL) was added cyclohexanecarbaldehyde (3.6 mL, 29.91 mmol) at room temperature. The resulting mixture was stirred at room temperature for 2 h. The solvent was removed by evaporation and CH3CN (150 mL) was added to the residue. Lead (IV) acetate (13.26 g, 29.91 mmol) was added as one portion under N2 and the resulting mixture was refluxed for 10 min. After cooling, the resulting solid was filtered and washed with CH3CN. To the filtrate was then added 3N NaOH (40 mL). The resulting mixture was stirred at 50° C. for 18 h. The solvent was removed by evaporation and the resulting residue was purified by flash chromatography on silica gel to yield 2-cyclohexyl-benzooxazole-6-carboxylic acid. MS m/z (M+H+) 246.2.
Workup
- customThe solvent was removed by evaporation and CH3CN (150 mL)
- additionwas added to the residue
- temperaturethe resulting mixture was refluxed for 10 min
- temperatureAfter cooling
- filtrationthe resulting solid was filtered
- washwashed with CH3CN
- additionTo the filtrate was then added 3N NaOH (40 mL)
- stirringThe resulting mixture was stirred at 50° C. for 18 h
- customThe solvent was removed by evaporation
- customthe resulting residue was purified by flash chromatography on silica gel
Sources & evidence
- ORD record
- ord-78b8116a48e745858fb971910dd6e93a
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08435977B2
Reaction notes
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