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[ CAS No. 39968-95-1 ] {[proInfo.proName]}

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Chemical Structure| 39968-95-1
Chemical Structure| 39968-95-1
Structure of 39968-95-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 39968-95-1 ]

CAS No. :39968-95-1 MDL No. :MFCD29920274
Formula : C14H26O4Si Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 286.44 Pubchem ID :-
Synonyms :

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Signal Word: Class:N/A
Precautionary Statements: UN#:N/A
Hazard Statements: Packing Group:N/A

Application In Synthesis of [ 39968-95-1 ]

* 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 [ 39968-95-1 ]

[ 39968-95-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 39968-95-1 ]
  • [ 551-11-1 ]
  • 2
  • [ 39746-00-4 ]
  • [ 39968-95-1 ]
  • 3
  • [ 32233-40-2 ]
  • [ 18162-48-6 ]
  • [ 39968-95-1 ]
YieldReaction ConditionsOperation in experiment
83% With 1H-imidazole In dichloromethane at 20℃; for 8h; 1.1; 2.1 (1) Synthesis of compound 2a Corinolone(20g, 116.2mmol) in dichloromethane (200ml) was added TBSCl (52.6g, 350mmol, 3.0eq), and imidazole (25.0g, 360mmol, 3.0eq), reacted at room temperature for 8h, suction filtered, added to the organic phase 10% hydrochloric acid solution (80mL), then react at room temperature for 5h, quench the reaction with saturated ammonium chloride solution (150ml), concentrate, add dichloromethane (200ml) and water (200ml), let stand for layer separation, the aqueous phase uses two Chloromethane (150ml*3) was extracted, washed with saturated brine (100ml), dried over anhydrous sodium sulfate, filtered, concentrated, and recrystallized from ethyl acetate (180ml) to obtain white solid compound 2 (27.4g, 83%).
82% With 1H-imidazole In dichloromethane at 20℃; for 8h; 1 To a solution of Coryrolactone (10 g, 58.1 mmol) in dichloromethane (100 mL) was added TBSCI (26.3 g, 175 mmol, 3.0 eq)And imidazole (12.5 g, 180 mmol, 3.0 eq),After reacting for 8 h at room temperature, suction-filtering, 10% hydrochloric acid solution (50 mL, 2.8 eq) was added to the organic phase, then reacted at room temperature for 5 h, quenched with saturated ammonium chloride solution (100 mL), concentrated, and then added dichloromethane (100 mL) Water (100mL), standing layered,The aqueous phase was extracted with dichloromethane (100 mL*3).Wash with saturated brine (100 mL) and dry over anhydrous sodium sulfate.Filtered, concentrated,Ethyl acetate (100ml)Recrystallization gave Compound 2a (13.6 g, 82%).
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