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Cyclohexane-1,1-dicarboxylic acid → Cyclohexane dicarboxylic acid molybdenum

HRID 343735
Notes
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Reaction equation

HRID 343735 reaction equation
[C:1]1([C:10]([OH:12])=[O:11])([C:7]([OH:9])=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C([O-])(=O)C.[Mo+4:17].C([O-])(=O)C.C([O-])(=O)C.C([O-])(=O)C>CO>[Mo:17].[C:1]1([C:10]([OH:12])=[O:11])([C:7]([OH:9])=[O:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 136906Cyclohexane-1,1-dicarboxylic acidHCID 11473018Molybdenum acetate

Product 1

HCID 88023834Cyclohexane dicarboxylic acid molybdenum

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

0.885 g (5.14 mmol) of cyclohexane dicarboxylic acid and 1,000 g (2.34 mmol) of molybdenum acetate were dissolved in 900 ml of methanol. After this was stirred for three days at the room temperature, this was kept still for a few days. Thereafter, its precipitation product was suction-filtered, rinsed sufficiently with methanol and then vacuum-dried for 60° C./4 hours, whereby 1.216 g of target substance was obtained. This substance had the specific surface area of 212 m2 /g. And, a measurement according to the HK method using argon revealed that the substance had the pore diameter of 5.2 Å.

Workup

  1. waitthis was kept still for a few days
  2. customThereafter, its precipitation product
  3. filtrationwas suction-filtered
  4. washrinsed sufficiently with methanol
  5. customvacuum-dried for 60° C./4 hours, whereby 1.216 g of target substance
  6. customwas obtained

Sources & evidence

ORD record
ord-c12d4ce02edf4c9ca761bddd0302cdb0
Source dataset
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05862796

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes