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Hydrogen Bromide → HCID 178514854, compound

HRID 1586293
Notes
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Reaction equation

HRID 1586293 reaction equation
Br.C[O:3][C:4]1[C:5](=[O:23])[C:6]2[C:14](=[CH:15][C:16]=1[O:17]C)[C:13]1[C:8](=[CH:9][C:10]([O:21]C)=[C:11]([O:19]C)[CH:12]=1)[CH:7]=2>C(O)(=O)C>[OH:3][C:4]1[C:5](=[O:23])[C:6]2[C:14](=[CH:15][C:16]=1[OH:17])[C:13]1[C:8](=[CH:9][C:10]([OH:21])=[C:11]([OH:19])[CH:12]=1)[CH:7]=2
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 260Hydrogen BromideHCID 675835612,3,6,7-Tetramethoxyfluorenone

Product 1

HCID 178514854HCID 178514854, compoundYield 76.9%

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

To a mixed solution of acetic acid (20 ml) and 47% hydrobromic acid (10 ml), 2,3,6,7-tetramethoxyfluorenone (8.0 g) was added and the mixture was refluxed for 15 hours. After cooling, the precipitated crystals were filtered, washed with water and then recrystallized from water-containing ethanol to give 5.0 g of 2,3,6,7-tetrahydroxyfluorenone as a claret powder.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. temperaturethe mixture was refluxed for 15 hours
  2. temperatureAfter cooling
  3. filtrationthe precipitated crystals were filtered
  4. washwashed with water
  5. customrecrystallized from water-
  6. additioncontaining ethanol

Sources & evidence

ORD record
ord-7588242036fc4364854fefaa810271f3
Source dataset
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05942641

Reaction notes

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