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[ CAS No. 24133-46-8 ] {[proInfo.proName]}

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Chemical Structure| 24133-46-8
Chemical Structure| 24133-46-8
Structure of 24133-46-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 24133-46-8 ]

CAS No. :24133-46-8 MDL No. :MFCD03425725
Formula : C6H12O3 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 132.16 Pubchem ID :-
Synonyms :

Safety of [ 24133-46-8 ]

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Application In Synthesis of [ 24133-46-8 ]

* 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 [ 24133-46-8 ]

[ 24133-46-8 ] Synthesis Path-Downstream   1~16

  • 1
  • [ 64-17-5 ]
  • [ 24133-46-8 ]
  • [ 70159-96-5 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid
  • 2
  • [ 135291-86-0 ]
  • [ 24133-46-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride
  • 3
  • [ 13361-35-8 ]
  • [ 13259-29-5 ]
  • [ 24133-46-8 ]
YieldReaction ConditionsOperation in experiment
With 2-methyl-propan-1-ol bei nachfolgendem Verseifen des entstandenen Esters mit konz.Kalilauge;
  • 4
  • [ 24133-46-8 ]
  • [ 140472-28-2 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride
  • 5
  • [ 24133-46-8 ]
  • [ 103860-78-2 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride Erhitzen des Reaktionsprodukts mit <i>sec</i>-Butylalkohol;
  • 6
  • [ 13259-29-5 ]
  • [ 79-11-8 ]
  • [ 24133-46-8 ]
YieldReaction ConditionsOperation in experiment
With 2-methyl-propan-1-ol
  • 7
  • [ 24133-46-8 ]
  • [ 100-63-0 ]
  • isobutoxy-acetic acid-(<i>N</i>'-phenyl-hydrazide) [ No CAS ]
YieldReaction ConditionsOperation in experiment
at 120℃;
  • 9
  • [ 78-83-1 ]
  • [ 105-36-2 ]
  • [ 24133-46-8 ]
YieldReaction ConditionsOperation in experiment
With sodium hydride In tetrahydrofuran
  • 10
  • [ 78-83-1 ]
  • [ 79-11-8 ]
  • [ 24133-46-8 ]
YieldReaction ConditionsOperation in experiment
With sodium 2.) reflux; Multistep reaction;
  • 12
  • [ 7719-09-7 ]
  • [ 24133-46-8 ]
  • [ 34180-11-5 ]
  • [ 56680-72-9 ]
  • [ 140472-28-2 ]
  • 13
  • [ 24133-46-8 ]
  • [ 56680-72-9 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride at 40 - 55℃;
  • 14
  • [ 24133-46-8 ]
  • [ 15268-49-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: SOCl2 / 40 - 55 °C 2: benzene
  • 15
  • [ 24133-46-8 ]
  • [ 189128-87-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: SOCl2 / 40 - 55 °C
  • 16
  • [ 78-83-1 ]
  • [ 3926-62-3 ]
  • [ 24133-46-8 ]
YieldReaction ConditionsOperation in experiment
With NaH In tetrahydrofuran; hexane; water; dimethyl sulfoxide 3 2-Methylpropoxyacetic acid STR12 EXAMPLE 3 2-Methylpropoxyacetic acid STR12 Sodium hydride (1.72 g of 60% NaH in oil=1.03 g, 43 mmol) in oil dispersion was washed twice with 10 ml of hexane. THF was added (10 ml) and the mixture was cooled to -15° C. A solution of 2-methyl propanol (2.5 g, 35 mmol) in THF was then added, and the mixture was warmed to 25° C. for 1 hour. The THF was removed by distillation under vacuum and a solution of sodium chloroacetate (5.2 g, 45 mmol) in DMSO (100 ml) was added. The mixture was stirred at room temperature for 20 hours, then diluted with 300 ml. of water. The mixture was extracted twice with 50 ml. of hexane. The agueous phase was acidified with 4 N hydrochloric acid and the product was extracted twice with 100 ml. of ethyl acetate. The combined ethyl acetate layers were washed twice with 100 ml. water, dried over MgSO4, filtered, and the solvent was removed by distillation under reduced pressure to give 4.6g of product as a colorless oil. Yield of product=99.6%.
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