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Chemical Structure| 732-80-9 Chemical Structure| 732-80-9

Structure of 732-80-9

Chemical Structure| 732-80-9

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Product Details of [ 732-80-9 ]

CAS No. :732-80-9
Formula : C16H16O3
M.W : 256.30
SMILES Code : O=C(C1=CC=C(C2=CC=C(OC)C=C2)C=C1)OCC
MDL No. :MFCD00671953
InChI Key :LGFDQZCUDVWAIQ-UHFFFAOYSA-N
Pubchem ID :2764348

Safety of [ 732-80-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 732-80-9 ]

* 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 [ 732-80-9 ]

[ 732-80-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 732-80-9 ]
  • [ 725-14-4 ]
YieldReaction ConditionsOperation in experiment
98.0% With sodium hydroxide; In tetrahydrofuran; Step B. 4'-Methoxy-[1,1'-biphenyl]-4-carboxylic Acid A solution of the ester of Step A (3.9 g, 15.2 mmol) in tetrahydrofuran (50 mL) was treated with 1 N sodium hydroxide (31 mL, 31 mmol) and then heated at reflux overnight. After cooling, the reaction mixture was concentrated in vacuo. The residue was acidified with 2N hydrochloric acid to give a white solid which was collected by filtration and dried under vacuum to provide the title compound (3.4 g, 98.0%) as a white solid, m.p. 250-254 C. 1H-NMR (DMSO-d6, 400 MHz): δ 3.81 (s, 3H), 7.04-7.08 (m, 2H), 7.68-7.71 (m, 2H), 7.73-7.77 (m, 2H), 7.98-8.01 (m, 2H), 12.91 (broad s, 1H). MS [(-)ESI, m/z]: 227 [M-H]-. Anal. Calcd. for C14H12O3: C, 73.67; H, 5.30. Found: C, 73.11; H, 5.41.
94% With sodium hydroxide; In methanol; water; Step 1: Ethyl-4'-methoxy-4-biphenylcarboxylate (1.29 g) was dissolved in methanol (7.5 mL) and sodium hydroxide (2 N in water, 7.5 mL) was added. The reaction was stirred at room temperature for 9 days and concentrated to dryness. Water (50 mL) was added and the mixture was made acidic with HCl (6 N in water). The precipitate was removed by filtration and dried under vacuum giving 4'-methoxy-4-biphenylcarboxylic acid (1.08 g). Yield=94%.
 

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