Sodium borohydride → 7-Fluorochroman-4-ol
Reaction equation
[F:1][C:2]1[CH:12]=[CH:11][C:5]2[C:6](=[O:10])[CH2:7][CH2:8][O:9][C:4]=2[CH:3]=1.[BH4-].[Na+]>CO>[F:1][C:2]1[CH:12]=[CH:11][C:5]2[CH:6]([OH:10])[CH2:7][CH2:8][O:9][C:4]=2[CH:3]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of 5.0 grams (0.03 mole) of 3,4-dihydro-7-fluoro-2H-1-benzopyran-4-one in 100 mL of methanol was added portionwise 3.4 grams (0.09 mole) of sodium borohydride during a one hour period, after which the reaction mixture was stirred for about 18 hours. The reaction mixture was then concentrated under reduced pressure to a residue, which was slurried in water and extracted with methylene chloride. The extract was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue, which was subjected to column chromatography on silica gel, with 1:4 ethyl acetate:hexane as the eluant. The product-containing fractions were combined and concentrated under reduce pressure, yielding 4.4 grams of 3,4-dihydro-7-fluoro-4-hydroxy-2H-1-benzopyran. The NMR spectrum was consistent with the proposed structure. This reaction was repeated several times.
Workup
- concentrationThe reaction mixture was then concentrated under reduced pressure to a residue, which
- extractionextracted with methylene chloride
- dry with materialThe extract was dried with magnesium sulfate
- filtrationfiltered
- concentrationThe filtrate was concentrated under reduced pressure to a residue, which
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-719a4dbe8bef4b2985bae2d722225c32
- Source dataset
- uspto-grants-1996_05
- Patent number
- US05521147
Reaction notes
Loading…