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Chemical Structure| 1092561-29-9 Chemical Structure| 1092561-29-9

Structure of 1092561-29-9

Chemical Structure| 1092561-29-9

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Product Details of [ 1092561-29-9 ]

CAS No. :1092561-29-9
Formula : C5H4ClNO2S
M.W : 177.61
SMILES Code : O=[N+](C1=CC(CCl)=CS1)[O-]
MDL No. :MFCD12197117

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Application In Synthesis of [ 1092561-29-9 ]

* 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 [ 1092561-29-9 ]

[ 1092561-29-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1092561-29-9 ]
  • [ 147751-16-4 ]
  • [ 1246278-16-9 ]
YieldReaction ConditionsOperation in experiment
74% With potassium carbonate; In ISOPROPYLAMIDE; at 50℃; for 16h; Part C. Preparation of fert-butyl methylsulfonyl((5-nitrothiophen-3-yl)methyl)carbamate. |00375| In a 50 mL round-bottomed flask was added the compound prepared in Part B (390 mg,2.196 mmol), methylsulfonylcarbamate (514 mg, 2.64 mmol), and potassium carbonate(303 mg, 2.196 mmol) in dimethylacetamide (10 mL) to give a brown suspension. The suspension was heated at 50 CC for 16 hours under nitrogen. The reaction mixture was cooled and partitioned between ethyl acetate and water. The ethyl acetate layer was washed with water and brine. The organic layer was dried over anhydrous ^SO4, filtered and concentrated in vacuo leaving a brown residue. The residue was purified by silica gel chromatography eluting with 1 :1 hexane/ethyl acetate and the title compound was obtained as a tan solid (0.55 g, 74%).
 

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