Sodium borohydride → 7-Fluorochroman-4-ol

HRID 440682Notes

Reaction equation

HRID 440682 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]=1

Participants

4

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

  1. concentrationThe reaction mixture was then concentrated under reduced pressure to a residue, which
  2. extractionextracted with methylene chloride
  3. dry with materialThe extract was dried with magnesium sulfate
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated under reduced pressure to a residue, which
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-719a4dbe8bef4b2985bae2d722225c32
Source dataset
uspto-grants-1996_05
Patent number
US05521147

Reaction notes

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