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Benzene → 1,4-Benzenedicarboxylic acid, 1-methyl ester, potassium salt (1:1)

HRID 46679
Notes
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Reaction equation

HRID 46679 reaction equation
[OH-].[K+:2].[C:3]([O:15]C)(=[O:14])[C:4]1[CH:13]=[CH:12][C:7]([C:8]([O:10][CH3:11])=[O:9])=[CH:6][CH:5]=1.C1C=CC=CC=1>CO>[C:8]([O:10][CH3:11])(=[O:9])[C:7]1[CH:12]=[CH:13][C:4]([C:3]([O-:15])=[O:14])=[CH:5][CH:6]=1.[K+:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 241BenzeneHCID 8441Dimethyl terephthalateHCID 14797Potassium Hydroxide

Product 1

HCID 236837531,4-Benzenedicarboxylic acid, 1-methyl ester, potassium salt (1:1)

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Potassium monomethyl terephthalate was prepared by adding dropwise a solution of 85.5 grams (1.286 mole) potassium hydroxide (85% pellets) in 675 ml methanol to a stirred solution of 250 grams (1.286 mole) of dimethyl terephthalate in 1600 ml. of benzene at 60° C. over 1 hour. The mixture was refluxed for 15 minutes, cooled, and filtered. The white solid on the filter was washed with acetone and sucked dry. It weighed 263 grams (93 mole % yield). It did not melt below 400° C.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. temperatureThe mixture was refluxed for 15 minutes
  2. temperaturecooled
  3. filtrationfiltered
  4. washThe white solid on the filter was washed with acetone
  5. customsucked dry
  6. custom263 grams (93 mole % yield)
  7. customdid not melt below 400° C.

Sources & evidence

ORD record
ord-b709ea5baacc4763b7e514f1fdf5cfa8
Source dataset
uspto-grants-1979_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04174447

Reaction notes

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