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Water → Monomethyl terephthalate

HRID 36487
Notes
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Reaction equation

HRID 36487 reaction equation
S(=O)(=O)(O)O.[OH2:6].[CH3:7][O:8][C:9](=[O:18])[C:10]1[CH:15]=[CH:14][C:13]([CH2:16][OH:17])=[CH:12][CH:11]=1>[O-2].[Cr+6].[O-2].[O-2].CC(C)=O>[CH3:7][O:8][C:9]([C:10]1[CH:15]=[CH:14][C:13]([C:16]([OH:6])=[O:17])=[CH:12][CH:11]=1)=[O:18]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 962WaterHCID 1118Sulfuric AcidHCID 81325Methyl 4-(hydroxymethyl)benzoate

Product 1

HCID 15513Monomethyl terephthalateYield 94%

Reagents, catalysts & solvents 2

HCID 10219390chromium (VI) trioxideCatalystHCID 180Acetone
Solvent

Procedure

Concentrated sulfuric acid (277.5 ml, 5.2 mol) was added dropwise over 1/2 hr to a stirred solution of chromium (VI) oxide (299.25 g, 2.99 mol) and water (925 ml) at 0°. The resulting solution was added dropwise over 1 hr to a stirred solution of methyl-4-(hydroxymethyl)benzoate (92.5 g, 0.564 mol) and acetone (4.6 1) at 0°. The reaction mixture was allowed to warm to room temperature and stirred overnight. The supernatant was decanted before the black tar-like residue was extracted with acetone. The decanted supernatant and acetone extracts were combined and concentrated under vacuum to leave a dark brown residue which was triturated with cold water (4 liter). The precipitate which formed was collected, washed three times with water (1 liter), and dried to give 94.6 g (94%) of the title compound as white crystals, m.p. 218°-221° C.

Workup

  1. customThe supernatant was decanted before the black tar-like residue
  2. extractionwas extracted with acetone
  3. concentrationconcentrated under vacuum
  4. customto leave a dark brown residue which
  5. customwas triturated with cold water (4 liter)
  6. customThe precipitate which formed
  7. customwas collected
  8. washwashed three times with water (1 liter)
  9. customdried

Sources & evidence

ORD record
ord-9c2c2a6a4c5b4e5cb20fc3b6992eaf8f
Source dataset
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05414132

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes