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Chemical Structure| 1174335-83-1 Chemical Structure| 1174335-83-1

Structure of 1174335-83-1

Chemical Structure| 1174335-83-1

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Product Details of [ 1174335-83-1 ]

CAS No. :1174335-83-1
Formula : C20H16ClNO5
M.W : 385.80
SMILES Code : O=C(C1=CC(N(C(CCl)=O)C/2=O)=C(C=C1)C2=C(OC)\C3=CC=CC=C3)OC

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Application In Synthesis of [ 1174335-83-1 ]

* 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 [ 1174335-83-1 ]

[ 1174335-83-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1174335-83-1 ]
  • [ 1168150-46-6 ]
YieldReaction ConditionsOperation in experiment
93.5% With methanol; potassium hydroxide; for 0.666667h;Reflux; l-(2-c oro-acetyl)-3-[l-methoxy-l-phenyl-meth-(E)-ylidene]-2-oxo-2,3-dihydro-lH- -6-carboxylic acid methyl ester (390.0 g / 1.0109 mol) was suspended in MeOH (1562 ml) and heated to reflux. A solution of KOH (23.35 g / 0.35 eq) in MeOH (196.8 ml) was added and the reaction was stirred for 40 minutes. After complete conversion the reaction was cooled down to 5C and stirred for an additional 30 minutes. The precipitated product was filtered off, washed with cold MeOH and dried under vacuum to obtain 292.2 g (93.5 %) of 3 - [ 1 -methoxy- 1 -phenyl-meth-(E)-ylidene] -2-oxo-2,3 -dihydro- 1 H-indole-6-carboxylic acid methyl ester.
With potassium hydroxide; In methanol; at 0℃; for 2.5h; Solution of KOH (41mg, 0.6mmol) in methanol (0.4 mL of) was added to 63 of (E)-1-cholroacetyl- 3-(methoxy(phenyl) methylene)-2-indolone-6- methyl formate (8-2) (800mg, 2mmol) in methanol 3.2mL) suspension of the reaction system was continued stirring for 30min, cooled to 0 C, and stirring was continued at 0 C for 2h, suction filtered, washed with methanol, and dried to give 600mg (94.6%) as a yellow solid, E)-methyl- 3-(methoxy(phenyl) methylene)-2-indolone-6- methyl formate (9-2).
 

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