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[ CAS No. 111934-94-2 ] {[proInfo.proName]}

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Chemical Structure| 111934-94-2
Chemical Structure| 111934-94-2
Structure of 111934-94-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 111934-94-2 ]

CAS No. :111934-94-2 MDL No. :MFCD20527801
Formula : C7H13BrO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 209.08 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 111934-94-2 ]

* 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 [ 111934-94-2 ]

[ 111934-94-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 4728-12-5 ]
  • [ 111934-94-2 ]
YieldReaction ConditionsOperation in experiment
100% With 1H-imidazole; carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20℃; for 4h;Cooling with ice; j0363] 2,2-Dimethyl-5-(hydroxymethyl)-1 ,3-dioxane (3a) (1.00 g) was dissolved in 22.8 mE of dichloromethane (MDC), and 700.0 mg of imidazole and 2.72 g of carbon tetrabromide were added thereto. After ice-cooling, 2.15 g of triphenylphosphine was thrther added, and the mixture was stirred at room temperature for 4 hours. Dichloromethane was distilled off under reduced pressure, and the resulting product was purified with silica gel chromatography (n-hexane:ethyl acetate=5: 1) to quantitatively obtain 1.60 g of 2,2-dimethyl-5-bromomethyl- 1 ,3-dioxane (Sb).
  • 2
  • [ 111934-95-3 ]
  • [ 111934-94-2 ]
  • [ 111934-96-4 ]
YieldReaction ConditionsOperation in experiment
27% With tert.-butyl lithium In diethyl ether 1.) -78 deg C, 12 min; 2.) 15 min;
  • 3
  • [ 51335-75-2 ]
  • [ 111934-94-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: 72 percent / 4 h / Heating 2: 82 percent / LiAlH4 3: 71 percent / pyridine, triphenylphosphine, carbon tetrabromide / CH2Cl2 / 2.5 h
Multi-step reaction with 4 steps 1: 65 percent / NaCl / H2O; dimethylsulfoxide / 6 h / Heating 2: 99 percent / LiAlH4 / diethyl ether / 2.5 h / Ambient temperature 3: triethylamine / 2.5 h / 0 °C 4: 24 percent / nBu4NBr / acetone / 1.5 h / Heating
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