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Chemical Structure| 114326-10-2 Chemical Structure| 114326-10-2

Structure of 114326-10-2

Chemical Structure| 114326-10-2

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Product Details of [ 114326-10-2 ]

CAS No. :114326-10-2
Formula : C9H17NO3S
M.W : 219.30
SMILES Code : O=C(SCCNC(OC(C)(C)C)=O)C
MDL No. :MFCD13195020

Safety of [ 114326-10-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 114326-10-2 ]

* 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 [ 114326-10-2 ]

[ 114326-10-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 158690-56-3 ]
  • [ 10387-40-3 ]
  • [ 114326-10-2 ]
YieldReaction ConditionsOperation in experiment
12 g With potassium carbonate; In dimethyl sulfoxide; at 15℃; for 2h; In a reaction flask, 2-[(tert-butoxycarbonyl)amino]ethyl 4-methylbenzensulphonate (18.00 g, 0.057 mol), dimethyl sulfoxide (95.00 ml) were loaded, the temperature was cooled to about 15 C., potassium carbonate (12.60 g, 0.091 mol) was added, potassium thioacetate (8.46 g, 0.074 mol) and the reaction mixture was maintained under these conditions for about two hours. Once the reaction is finished, a mixture of water and ice (114 g) was added at the temperature of about 10 C. and the aqueous phase was extracted with toluene (2*72 ml). The organic phase was washed with water (4*36 ml) and the collected organic phase were concentrated till residue through vacuum distillation to give 12 g di S-2-(tert-butoxycarbonyl amino)ethyl-ethantionate. 1H-NMR (CDCl3, 300 MHz): δ 3.25 (t, 2H), 2.97 (t, 2H), 2.31 (s, 3H), 1.43 (s, 9H).
 

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