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Chemical Structure| 7500-53-0 Chemical Structure| 7500-53-0
Chemical Structure| 7500-53-0

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Synonyms: 1,2-Benzenediacetic acid

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Product Details of o-Phenylenediacetic acid

CAS No. :7500-53-0
Formula : C10H10O4
M.W : 194.18
SMILES Code : O=C(O)CC1=CC=CC=C1CC(O)=O
Synonyms :
1,2-Benzenediacetic acid
MDL No. :MFCD00004329
InChI Key :MMEDJBFVJUFIDD-UHFFFAOYSA-N
Pubchem ID :24123

Safety of o-Phenylenediacetic acid

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of o-Phenylenediacetic acid

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 7500-53-0 ]

[ 7500-53-0 ] Synthesis Path-Downstream   1~1

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  • [ 613-73-0 ]
  • [ 7500-53-0 ]
YieldReaction ConditionsOperation in experiment
56% With hydrogenchloride; water;Reflux; Example No.3. Synthesis of 2,2'-(l,2-phenylene)diacetic acid.[0055] The above dinitrile was dissolved in 50 mL concentrated HC1 and refluxed for 3 h. Water (30 mL) was added and the reaction heated overnight, then cooled and washed with ether. The organic layer was extracted twice with sodium carbonate. Combined aqueous layers were acidified and extracted with ether, which was dried (MgSO4), filtered and concentrated. The diacid was obtained as a pale yellow solid in 56% yield: mp 123 - 125 C; 1H NMR (250 MHz, DMSO-D6) 5 3.58 (s, 4H), 7.20 (s, 4H), 12.34 (br s, 2H); 13C NMR (63 MHz, DMSO-D6) 37.1 (2C), 126.8 (2C), 130.6 (2C), 134.1 (2C), 172.4 (2C).
With sulfuric acid; water; for 2h;Heating / reflux; Example 1; Preparation of 1,2-Phenylenediacetic acid (compound 2); In a round-bottomed flask, fitted with a reflux condenser, 10 g of phenylenediacetonitrile and 180 g of 50% sulphuric acid were refluxed for 2 h. The reaction mixture was cooled on ice to yield (2) as white crystals. Yield 11.4 g. This compound was used without further purification.
 

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