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Chemical Structure| 1195529-07-7 Chemical Structure| 1195529-07-7

Structure of 1195529-07-7

Chemical Structure| 1195529-07-7

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Product Details of [ 1195529-07-7 ]

CAS No. :1195529-07-7
Formula : C17H11NO4
M.W : 293.27
SMILES Code : O=C(ON(C(C1=C2C=CC=C1)=O)C2=O)/C=C/C3=CC=CC=C3
English Name :1,3-Dioxoisoindolin-2-yl cinnamate
MDL No. :MFCD00405209
InChI Key :RWBPSIPMHURWQQ-ZHACJKMWSA-N
Pubchem ID :6008258

Safety of [ 1195529-07-7 ]

Application In Synthesis of [ 1195529-07-7 ]

* 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 [ 1195529-07-7 ]

[ 1195529-07-7 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 524-38-9 ]
  • [ 140-10-3 ]
  • [ 1195529-07-7 ]
YieldReaction ConditionsOperation in experiment
89% With dmap; dicyclohexyl-carbodiimide In 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran at 20℃; for 2h; Schlenk technique; Inert atmosphere;
87% With dmap; dicyclohexyl-carbodiimide In tetrahydrofuran at 20℃; for 15h;
68% With triethylamine In 2-methyltetrahydrofuran; ethyl acetate at 60℃; for 24h; Sealed tube; Green chemistry; General procedure for the preparation of N-(acyloxy)phthalimides (1). General procedure: In a sealed vial, N-hydroxyphthalimide (13, 2.0 mmol) or N-hydroxy compounds (15, 2.0 mmol), the corresponding carboxylic acid (14, 2.0 mmol), T3P (50% in EtOAc, 1.41 mL, 2.4 mmol, 1.2 equiv.) and triethylamine (0.333 mL, 2.4 mmol, 1.2 equiv.) were dissolved in 2-Me-THF (10 mL). The mixture was stirred at room temperature or at 60 °C for 2448 h. After the reaction was complete (followed by TLC, hexaneEtOAc 4:1), 2-Me-THF (50 mL) was added to the mixture and the organic phase was extracted with a 5% NaHCO3 solution (50 mL) and washed with distilled water (50 mL). The organic layer was dried over Na2SO4 and after filtration, the volatiles were evaporated. Analytical samples were purified by recrystallization from the solvent given below after the melting point. Compounds 1am, 1q, 1t and 17a are known from the literature, while 1np, 1r, 1s and 17b are new substances
47 % With dmap; diisopropyl-carbodiimide In dichloromethane at 18℃; Inert atmosphere;

  • 2
  • [ 1195529-07-7 ]
  • [ 73183-34-3 ]
  • [ 83947-56-2 ]
YieldReaction ConditionsOperation in experiment
48% With isonicotinate tert-butyl ester at 110℃; for 15h; Schlenk technique; Inert atmosphere;
  • 3
  • [ 14371-10-9 ]
  • [ 524-38-9 ]
  • [ 1195529-07-7 ]
YieldReaction ConditionsOperation in experiment
45% With Iron(III) nitrate nonahydrate In acetonitrile at 80℃; for 1h; Green chemistry;
  • 4
  • [ 524-38-9 ]
  • [ 4407-36-7 ]
  • [ 1195529-07-7 ]
YieldReaction ConditionsOperation in experiment
20% With Iron(III) nitrate nonahydrate In acetonitrile at 80℃; for 24h; Green chemistry;
  • 5
  • [ 140-10-3 ]
  • [ 1195529-07-7 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: pyridine; thionyl fluoride / acetonitrile / 1 h / 20 °C / Sealed tube 2: acetonitrile / 1 h / 20 °C
  • 6
  • [ 524-38-9 ]
  • [ 38986-89-9 ]
  • [ 1195529-07-7 ]
YieldReaction ConditionsOperation in experiment
288 mg In acetonitrile at 20℃; for 1h;
  • 7
  • [ 1195529-07-7 ]
  • [ 91-64-5 ]
YieldReaction ConditionsOperation in experiment
17% With caesium carbonate; 4-hydroxy-3-(phenylthio)-2H-chromen-2-one In acetonitrile at 35℃; for 16h; Irradiation;
 

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