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Chemical Structure| 54441-66-6 Chemical Structure| 54441-66-6

Structure of 54441-66-6

Chemical Structure| 54441-66-6

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Product Details of [ 54441-66-6 ]

CAS No. :54441-66-6
Formula : C13H16O3
M.W : 220.26
SMILES Code : O=C(OC(C)(C)C)CC(C1=CC=CC=C1)=O
MDL No. :MFCD00760727

Safety of [ 54441-66-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 54441-66-6 ]

* 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 [ 54441-66-6 ]

[ 54441-66-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 54441-66-6 ]
  • [ 2156-56-1 ]
  • 4-[(benzoyl)(tert-butoxycarbonyl)methylene]-1,3-dithietane-2-carboxylic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; carbon disulfide; In hexane; tert-butyl alcohol; benzene; REFERENCE EXAMPLE 3 STR31 In a mixture of 2.2 g. of tert-butyl benzoylacetate and 20 ml. of tert-butanol was dissolved 0.24 g. of sodium hydride (50% in oil), and 0.6 ml. of carbon disulfide was added to the solution at 15-20 C. followed by stirring for 40 minutes, 0.24 g. of sodium hydride (50% in oil) was then added to the mixture followed by stirring for one hour. To the reaction mixture obtained was added 1.52 g. of <strong>[2156-56-1]sodium dichloroacetate</strong> followed by stirring for 4 hours at room temperature. The reaction mixture was concentrated under reduced pressure and after adding 30 ml. of 1 normal hydrochloric acid to the residue formed, the product was extracted with 30 ml. of benzene. The extract was washed with water, dried, and concentrated under reduced pressure. By adding a mixture of benzene and n-hexane of 3:1 by volume ratio to the residue formed, 0.9 g. of the yellowish crystals of 4-[(benzoyl)(tert-butoxycarbonyl)methylene]-1,3-dithietane-2-carboxylic acid were obtained.
With hydrogenchloride; carbon disulfide; In hexane; tert-butyl alcohol; benzene; EXAMPLE 10 STR47 In a mixture of 2.2 g. of tert-butyl benzoylacetate and 20 ml. of tert-butanol was dissolved in 0.24 g. of sodium hydride (50% in oil), and 0.6 ml. of carbon disulfide was added to the solution at 15-20 C. followed by stirring for 40 minutes, and then 0.24 g. of sodium hydride (50% in oil) was added to the mixture followed by stirring for one hour. To the reaction mixture obtained was added 1.52 g. of <strong>[2156-56-1]sodium dichloroacetate</strong> followed by stirring for 4 hours at room temperature. The reaction mixture was concentrated under reduced pressure and after adding 30 ml. of 1 normal hydrochloric acid to the residue formed, the product was extracted with 30 ml. of benzene. The extract was washed with water, dried, and concentrated under reduced pressure. By adding a mixture of benzene and n-hexane of 3:1 by volume ratio to the residue formed, 0.9 g. of the yellowish crystals of 4-[(benzoyl)(tert-butoxycarbonyl)methylene]-1,3-dithietane-2-carboxylic acid were obtained. Melting point: 147-148 C. (decomposed) Nuclear magnetic resonance spectra (CDCl3)
 

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