Sodium borohydride → HCID 19699318, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[F:11])[C:7](=[O:12])[CH2:6][CH2:5]2.[BH4-].[Na+]>C(O)C>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[F:11])[CH:7]([OH:12])[CH2:6][CH2:5]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5,6-Difluoroindan-1-one (59.3 g, 0.353 mol) was dissolved in 1 L of ethanol and sodium borohydride (6.68 g, 0.176 mol) was added. The mixture was stirred for 48 hours and the ethanol was removed by evaporation under reduced pressure. The residue was partitioned between diethyl ether and water and the mixture was acidified with 1N hydrochloric acid. The mixture was dried over magnesium sulfate and filtered. The solvents were evaporated giving 5,6-difluoro-1-hydroxyindane (59.8 g) as an oil.
Workup
- customthe ethanol was removed by evaporation under reduced pressure
- customThe residue was partitioned between diethyl ether and water
- dry with materialThe mixture was dried over magnesium sulfate
- filtrationfiltered
- customThe solvents were evaporated
Sources & evidence
- ORD record
- ord-d56174c1718445edab3ca27d48ff8d9b
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05719280
Reaction notes
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