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Chemical Structure| 10599-72-1 Chemical Structure| 10599-72-1

Structure of 10599-72-1

Chemical Structure| 10599-72-1

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Product Details of [ 10599-72-1 ]

CAS No. :10599-72-1
Formula : C10H12O3
M.W : 180.20
SMILES Code : CC(=O)C1=C(C)OC(C)=C1C(C)=O

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Application In Synthesis of [ 10599-72-1 ]

* 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 [ 10599-72-1 ]

[ 10599-72-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5027-32-7 ]
  • [ 10599-72-1 ]
YieldReaction ConditionsOperation in experiment
87.6% With potassium hydrogensulfate; In 5,5-dimethyl-1,3-cyclohexadiene;Heating; action apparatus was a 2000 ml four-neck round bottom flask equipped with a thermometer, a mechanical stirrer, a water separator, a condenser, and a silicone oil bath.The four-necked round bottom flask was placed in a silicone oil bath, and the thermometer and water separator were mounted on a four-neck round bottom flask. The condenser was installed at the upper end of the water separator, and 198 g of 3 was placed in a 2000 ml four-neck round bottom flask. 4-diacetyl-2,5-hexanedione, 1000ml of xylene and 6.8g of potassium hydrogen sulfate, start stirring with a stirrer, warm the water in a silicone oil bath and return to water until no water is released, stop heating, cool to room temperature, filter The catalyst was removed, and the filtrate was evaporated under reduced pressure to dryness crystals crystals crystals crystals 87.6%, the mother liquor is applied later.
68% With titanium tetrachloride; In toluene; at 80℃;Inert atmosphere; In a 50 mL two-necked flask equipped with a reflux condenser and under the protection of nitrogen,Add freshly distilled toluene(20 mL), tetracarbonyl compound 1a (5 mmol) and titanium tetrachloride (10 mmol).Heated to 80 C with stirring for 0.5-2 hours,The reaction was monitored continuously by TLC, quenched by addition of saturated aqueous ammonium chloride (10 mL)Two-phase solution was obtained.A separatory funnel was used to separate the upper toluene solution,The lower aqueous solution was extracted with dichloromethane (3 × 10 mL).The resulting toluene and methylene chloride solution were combined,Dried over anhydrous sodium sulfate and concentrated under reduced pressure,Directly silica gel column chromatography,Furan IIa was obtained as a yellow oil in 68% yield.
In hydrogenchloride; A mixture of 1.0 g. of 1,1,2,2-tetraacetylethane in 10 ml. of concentrated hydrochloric acid was stirred at room temperature for about 1 hour until a clear solution was obtained. The mixture was then poured onto ice and extracted with diethyl ether. The extracts were dried over sodium sulfate, taken to dryness, and the residue recrystallized from hexane to give 2,5-dimethyl-3,4-diacetylfuran, m.p. 75-77 C.
 

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