| Identification | Back Directory | [Name]
2 - Methyl - 2 - (2 - phthaliMidoethyl) - 1,3 - dioxolane | [CAS]
84764-41-0 | [Synonyms]
2 - Methyl - 2 - (2 - phthaliMidoethyl) - 1,3 - dioxolane 2-[2-(2-Methyl-1,3-dioxolan-2-yl)ethyl]isoindole-1,3-dione 2-(2-(2-Methyl-1,3-dioxolan-2-yl)ethyl)isoindoline-1,3-dione 1H-Isoindole-1,3(2H)-dione, 2-[2-(2-methyl-1,3-dioxolan-2-yl)ethyl]- 2-[2-(2-Methyl-1,3-Dioxolan-2-Yl)Ethyl]Isoindoline-1,3-Dione(WXC00028) | [Molecular Formula]
C14H15NO4 | [MDL Number]
MFCD09923388 | [MOL File]
84764-41-0.mol | [Molecular Weight]
261.27 |
| Chemical Properties | Back Directory | [Melting point ]
122 °C(Solv: ethanol (64-17-5)) | [Boiling point ]
381.9±17.0 °C(Predicted) | [density ]
1.271±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
-2.11±0.20(Predicted) | [Appearance]
Light yellow to yellow Solid |
| Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of 2-(2-(2-methyl-1,3-dioxolan-2-yl)ethyl)isoindoline-1,3-dione from 2-(3-oxobutyl)isoindoline-1,3-dione and ethylene glycol is as follows: 50 g of 2-(3-oxobutyl)isoindoline-1,3-dione, 14.3 g of ethylene glycol, and 7.4 g of p-toluenesulphonium tetrahydrate of the The mixture was dissolved in 500 mL of anhydrous toluene, a water separator was assembled and the reaction was refluxed for 24 hours. Upon completion of the reaction, the reaction mixture was washed twice with 500 mL of saturated aqueous NaHCO3. The aqueous phase was extracted twice with 500 mL of ethyl acetate. The organic phases were combined, dried by adding anhydrous sodium sulfate and the solvent was removed by distillation under reduced pressure. The resulting distillation residue was recrystallized from ethanol to give 45 g of the yellow solid product 2-(2-(2-methyl-1,3-dioxolan-2-yl)ethyl)isoindoline-1,3-dione in 74.8% yield. | [References]
[1] Patent: CN106939001, 2017, A. Location in patent: Paragraph 0007 [2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1986, p. 1533 - 1540 [3] Journal of the Chemical Society, 1955, p. 3151,3153 [4] Synlett, 2003, # 7, p. 987 - 990 |
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