Phosphate → 9H-Fluoren-9-one, 6-bromo-2-(hydroxymethyl)-

HRID 1707991Notes

Reaction equation

HRID 1707991 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6](=[O:20])[C:7]3[C:12]([C:13]=2[CH:14]=1)=[CH:11][CH:10]=[C:9]([CH2:15][O:16]C(=O)C)[CH:8]=3.C[O-].[Na+].P([O-])([O-])([O-])=O>CO.C1COCC1.C(OCC)(=O)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6](=[O:20])[C:7]3[C:12]([C:13]=2[CH:14]=1)=[CH:11][CH:10]=[C:9]([CH2:15][OH:16])[CH:8]=3

Participants

7

Reactant 3

HCID 1061PhosphateHCID 10758857HCID 10758857, compoundHCID 10942334Sodium Methoxide

Product 1

HCID 105414109H-Fluoren-9-one, 6-bromo-2-(hydroxymethyl)-Yield 97.1%

Reagents, catalysts & solvents 3

HCID 887MethanolSolventHCID 8028TetrahydrofuranSolventHCID 8857Ethyl AcetateSolvent

Procedure

3-Bromo-7-acetoxymethyl-9-fluorenone (1.18 g) was suspended in methanol (102 ml) and THF (23 ml). To this suspension was added 0.054M NaOMe (6.6 ml). The reaction mixture was stirred at room temperature for 1.25 hours. It was then neutralized with 0.2M pH 7 phosphate buffer. The tetrahydrofuran and methanol were removed under reduced pressure. Reaction mixture was then diluted with ethyl acetate, washed with water and brine, dried and evaporated which gave the product (1.0 g).

Workup

  1. customThe tetrahydrofuran and methanol were removed under reduced pressure
  2. customReaction mixture
  3. washwashed with water and brine
  4. customdried
  5. customevaporated which

Sources & evidence

ORD record
ord-41f0f1f1f9c54b9f9fd38da817fd0596
Source dataset
uspto-grants-1994_10
Patent number
US05356889

Reaction notes

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