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Chemical Structure| 2237-36-7 Chemical Structure| 2237-36-7
Chemical Structure| 2237-36-7

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4-Methoxysalicylic acid, an arabinose derivative, is used in the synthesis of 1,3,4-oxadiazole derivatives.

Synonyms: 4-Methoxysalicylic Acid; 2-Hydroxy-p-anisic Acid

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Product Details of 2-Hydroxy-4-methoxybenzoic acid

CAS No. :2237-36-7
Formula : C8H8O4
M.W : 168.15
SMILES Code : COC1=CC(O)=C(C=C1)C(O)=O
Synonyms :
4-Methoxysalicylic Acid; 2-Hydroxy-p-anisic Acid
MDL No. :MFCD00002450
InChI Key :MRIXVKKOHPQOFK-UHFFFAOYSA-N
Pubchem ID :75231

Safety of 2-Hydroxy-4-methoxybenzoic acid

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

Application In Synthesis of 2-Hydroxy-4-methoxybenzoic 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 [ 2237-36-7 ]

[ 2237-36-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2237-36-7 ]
  • [ 112734-22-2 ]
  • [ 541-41-3 ]
  • [ 314297-97-7 ]
YieldReaction ConditionsOperation in experiment
36% With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; Step 1: 3-(4-Bromo-2-fluoro-benzyl)-7-methoxy Benzo[e][1,3]oxazine-2,4-dione: A solution of 2-hydroxy-4-methoxybenzoic acid (2.04 g, 12.2 mmol) in tetrahydrofuran (20 mL, 0.6 M) was cooled to 0° C. After being treated with diisopropylethylamine (4.4 mL, 25.3 mmol) and ethyl chloroformate (2.4 mL, 25.1 mmol), the mixture was stirred at room temperature for 1 h and subsequently treater with a solution of <strong>[112734-22-2]2-fluoro-4-bromobenzylamine</strong> (2.92 g, 12.1 mmol) and diisopropylethylamine (4.4 mL, 25.3 mmol) in tetrahydrofuran (15 mL). After stirring at room temperature for 22 h, the reaction mixture was diluted ethyl acetate and successively washed with 2 N HCl, saturated aq NaHCO3 and saturated aq NaCl. The organic layer was dried over Na2SO4, filtered and concentrated. The crude solid was purified by recrystallization with heptane and ethyl acetate to give 3-(4-bromo-2-fluoro-benzyl)-7-methoxy benzo[e][1,3]oxazine-2,4-dione (1.68 g, 36percent): 1H NMR (DMSO-d6, 300 MHz) delta 7.87 (d, J=8.4 Hz, 1H), 7.53 (dd, J1=10.5 Hz, J2=1.1 Hz, 1H), 7.33-7.34 (m, 2H), 7.03-6.99 (m, 2H), 5.02 (s, 2H), 3.87 (s, 3H).
 

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