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Chemical Structure| 15678-99-6 Chemical Structure| 15678-99-6

Structure of 15678-99-6

Chemical Structure| 15678-99-6

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Product Details of [ 15678-99-6 ]

CAS No. :15678-99-6
Formula : C6H12ClNO
M.W : 149.62
SMILES Code : O=C(NC(C)(C)C)CCl
MDL No. :MFCD00032565
InChI Key :NQVPSGXLCXZSTB-UHFFFAOYSA-N
Pubchem ID :222440

Safety of [ 15678-99-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501

Application In Synthesis of [ 15678-99-6 ]

* 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 [ 15678-99-6 ]

[ 15678-99-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15678-99-6 ]
  • [ 1196473-37-6 ]
  • [ 1268390-42-6 ]
YieldReaction ConditionsOperation in experiment
35.4% H181 (0.333mmol) was dissolved in DMSO (5mL). To this solution under nitrogen were added potassium carbonate (184mg, 1.333mmol, 4.0eq), a catalytic amount of Nal and N-tert-butyl-2-chloroacetamide (199mg, 1.333mmol, 4.0eq). The reaction mixture was stirred for 15 hours at 90°C then treated with 1M HC1 (10ml). After extraction with ethyl acetate, the organic layer was washed with water and brine, and dried over anhydrous Na2S04. The residue after rotary evaporation was purified by column chromatography over silica gel and recrystallization to give the title compound (31mg, 35.4percent yield). 1H NMR (400 MHz, DMSO-d6): delta 9.13 (s, 1H), 7.41 (s, 1H), 7.32 (d, J = 8.4 Hz, 1H), 7.22 (s, 1H), 7.07 (d, J = 8.4 Hz, 1H), 4.92 (s, 2H), 4.39 (s, 2H) and 1.29 (s, 9H) ppm. Mp 149-150°C.
 

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