2-Acetoxymethyl-4-cyclopropylmethoxy pyridine → 4-Cyclopropylmethoxy-2-hydroxymethylpyridine
Reaction equation
C([O:4][CH2:5][C:6]1[CH:11]=[C:10]([O:12][CH2:13][CH:14]2[CH2:16][CH2:15]2)[CH:9]=[CH:8][N:7]=1)(=O)C>[OH-].[Na+]>[CH:14]1([CH2:13][O:12][C:10]2[CH:9]=[CH:8][N:7]=[C:6]([CH2:5][OH:4])[CH:11]=2)[CH2:15][CH2:16]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
To the crude 2-acetoxymethyl-4-cyclopropylmethoxy pyridine, NaOH (100 ml 2 M) was added and the mixture was refluxed for 2 hours. The mixture was extracted with methylene chloride, and the phases were separated. The organic layer was dried with Na2SO4, filtered and the solvent was evaporated off, yielding 2.7 g of crude title compound. NMR data is given below. The crude product was used without any further purification.
Workup
- temperaturethe mixture was refluxed for 2 hours
- extractionThe mixture was extracted with methylene chloride
- customthe phases were separated
- dry with materialThe organic layer was dried with Na2SO4
- filtrationfiltered
- customthe solvent was evaporated off
Sources & evidence
- ORD record
- ord-645f1a8028f04acda2962272f5a21e4a
- Source dataset
- uspto-grants-1991_08
- Patent number
- US05039808
Reaction notes
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