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Chemical Structure| 1114-92-7 Chemical Structure| 1114-92-7

Structure of 1114-92-7

Chemical Structure| 1114-92-7

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Product Details of [ 1114-92-7 ]

CAS No. :1114-92-7
Formula : C8H14O4
M.W : 174.19
SMILES Code : CC(OC(C)=O)C(OC(C)=O)C
English Name :Butane-2,3-diyl diacetate
MDL No. :MFCD24038916

Safety of [ 1114-92-7 ]

Application In Synthesis of [ 1114-92-7 ]

* 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 [ 1114-92-7 ]

[ 1114-92-7 ] Synthesis Path-Downstream   1~14

  • 2
  • [ 5780-13-2 ]
  • [ 415974-43-5 ]
  • [ 1114-92-7 ]
YieldReaction ConditionsOperation in experiment
With acetic acid at 100 - 110℃; diacetate of meso-2.3-butylene glycol;
  • 3
  • [ 598-71-0 ]
  • [ 415974-43-5 ]
  • [ 1114-92-7 ]
YieldReaction ConditionsOperation in experiment
With acetic acid at 100 - 110℃; (+-)-<i>threo</i>-butanediol-(2.3)-diacetate;
  • 4
  • [ 1114-92-7 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Pyrolysis; substance uncertain configuration;
at 630℃; Pyrolysis; Flow reactor; 3 Example 3-Pyrolysis of 2,3-Butanediol Diacetate A feedstock that consists of 2,3-butanediol diacetate feeds a pyrolysis oven. The temperature of the pyrolysis oven is regulated in such a way as to obtain a reactor outlet temperature of 630° C. The flow rate of 2,3-butanediol diacetate is regulated to obtain a dwell time of between 0.9 and 1.5 seconds. The pyrolysis effluent is quickly cooled to 45° C. with a condenser placed right at the exit from the pyrolysis oven. The conversion of 2,3-butanediol diacetate varies between 96.5% and 99.1% based on the dwell time. The selectivity of transformation of 2,3-butanediol diacetate into 1,3-butadiene is between 78% and 82%. The selectivity of transformation of 2,3-butanediol diacetate into intermediate pyrolysis compounds varies between 17.2% and 20.0%. The selectivity of transformation of 2,3-butanediol diacetate into MEK varies between 0.9% and 1.8%. There is no other conversion product detected.
Pyrolysis; substance uncertain configuration;
  • 5
  • [ 5341-95-7 ]
  • [ 108-24-7 ]
  • [ 1114-92-7 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid diacetate of meso-2.3-butylene glycol;
  • 6
  • [ 19132-06-0 ]
  • [ 108-24-7 ]
  • [ 1114-92-7 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid (+-)-<i>threo</i>-butanediol-(2.3)-diacetate;
  • 7
  • [ CAS Unavailable ]
  • [ 513-85-9 ]
  • [ 1114-92-7 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid substance uncertain configuration;
  • 8
  • [ 5341-95-7 ]
  • [ 75-36-5 ]
  • [ 1114-92-7 ]
YieldReaction ConditionsOperation in experiment
With pyridine diacetate of meso-2.3-butylene glycol;
With 2,3-Dimethylaniline diacetate of meso-2.3-butylene glycol;
  • 9
  • [ 19132-06-0 ]
  • [ 75-36-5 ]
  • [ 1114-92-7 ]
YieldReaction ConditionsOperation in experiment
With 2,3-Dimethylaniline (+-)-<i>threo</i>-butanediol-(2.3)-diacetate;
With pyridine (+-)-<i>threo</i>-butanediol-(2.3)-diacetate;
  • 10
  • [ 590-18-1 ]
  • [ CAS Unavailable ]
  • [ 1114-92-7 ]
YieldReaction ConditionsOperation in experiment
With tellurium oxide; lithium bromide
  • 11
  • [ CAS Unavailable ]
  • [ CAS Unavailable ]
  • [ 1114-92-7 ]
YieldReaction ConditionsOperation in experiment
With tellurium oxide; lithium bromide
  • 12
  • [ 9003-20-7 ]
  • [ 1114-92-7 ]
YieldReaction ConditionsOperation in experiment
With hydrogen; mercury at 20℃; for 20h; Irradiation; Title compound not separated from byproducts;
  • 13
  • [ 1114-92-7 ]
  • [ 563-84-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride at 30℃; for 168h;
  • 14
  • [ 1114-92-7 ]
  • [ 56255-48-2 ]
  • [ 513-85-9 ]
YieldReaction ConditionsOperation in experiment
1: 39% 2: 31% In methanol; chloroform for 312h; Ambient temperature;
 

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