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Chemical Structure| 7159-95-7 Chemical Structure| 7159-95-7

Structure of 7159-95-7

Chemical Structure| 7159-95-7

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Product Details of [ 7159-95-7 ]

CAS No. :7159-95-7
Formula : C9H11NO3
M.W : 181.19
SMILES Code : O=C(OCC)NC1=CC=C(O)C=C1
MDL No. :MFCD11167769
Boiling Point : No data available

Safety of [ 7159-95-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 7159-95-7 ]

* 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 [ 7159-95-7 ]

[ 7159-95-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7159-95-7 ]
  • [ 117011-70-8 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide; sodium hydroxide; In chloroform; water; acetone; 2-(4-aminophenoxy)2-methylpropionic acid 4-ethoxycarbonylaminophenol 6.335 g (0.035 mole) and 7.5 g NaOH were added to 30 ml acetone. To the refluxing mixture 2.5 ml chloroform were dropwise added. While the mixture was stirring, it was refluxed for four hours. Excess of the solvent was evaporated. The residue was dissolved in water and acidified. A light brown oil was obtained which slowly turned to a crystalline mass 4.5 g (48%) mP 82-83. The above ester was boiled with 45 ml 10% KOH in water for half hour. After cooling, the reaction mixture was acidified with concentrated acetic acid to give 2.86 g (87%) of desired compound. This compound may be reacted with the isocyanate as in Example 1 to form the same product of Example 1.
With potassium hydroxide; sodium hydroxide; In chloroform; water; acetone; EXAMPLE 3 2-(4-aminophenoxy)-2-methylpropionic acid To a refluxing mixture of 4-ethoxycarbonylaminophenol 12.67 g (0.07 mole) and 15 g NaOH in 60 ml acetone, 5 ml chloroform were dropwise added. Stirring and refluxing continued for 4 hours. At the end, excess of acetone was evaporated. A solution of 20 g KOH in 75 ml water was added and boiled for half hour. After cooling, the solution was acidified with acetic acid to give 2-(4-aminophenoxy)-2-methylpropionic acid as a white crystalline compound, 7.15 g (51%), MP 216-218.
 

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