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Chemical Structure| 6855-48-7 Chemical Structure| 6855-48-7

Structure of 6855-48-7

Chemical Structure| 6855-48-7

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Product Details of [ 6855-48-7 ]

CAS No. :6855-48-7
Formula : C8H7NO2
M.W : 149.15
SMILES Code : O=C1NC2=C(C=CC(O)=C2)C1
MDL No. :MFCD05663501
InChI Key :ZOJZYAPVVOLQQB-UHFFFAOYSA-N
Pubchem ID :2784139

Safety of [ 6855-48-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 6855-48-7 ]

* 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 [ 6855-48-7 ]

[ 6855-48-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17641-08-6 ]
  • [ 6855-48-7 ]
YieldReaction ConditionsOperation in experiment
62% 2) <strong>[17641-08-6]2-chloro-N-(3-methoxyphenyl)acetamide</strong> (3.1g, 16 mmol) and anhydrous AlCl3 powder (4.4g,32 mmol) is heated and stirred at 120C for 10 minutes and exhibit a melting state. The temperature is elevated gradually to 240C in 40 minutes and then stirred 5 minutes. The reaction is allowed to cool to obtain a brown powder. The solid powder is poured into a mixture of 100g of crushed ice and 50ml of concentrated hydrochloric acid. The mixture is stirred for 10 minutes and then reflux for 10 minutes, and allowed to cool to precipitate a light yellow powder, which is filtered out and recrystallized in water to obtain 1.5g of 6-hydroxy-indoline-2-one, with a yield of 62%.
62% With aluminum (III) chloride; at 120℃; for 0.166667h; <strong>[17641-08-6]2-chloro-N-(3-methoxyphenyl)acetamide</strong> (3.1 g, 16 mmol) and anhydrous AlCl 3 powder (4.4 g, 32 mmol) were heated and stirred at 120 C. for 10 minutes,The melted state was allowed to appear, the temperature was gradually increased to 240 C. over 40 minutes, stirred for 5 minutes and allowed to cool to obtain a brown powder, the solid powder was poured into a mixture of 100 g of crushed ice and 50 ml of concentrated hydrochloric acid , Stirred for 10 minutes, then refluxed for 10 minutes, cooled, precipitated a light yellow powder, filtered and recrystallized from water,1.5 g of 6-hydroxy-indolin-2-one are obtained. Yield is 62%.
 

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