Home Cart 0 Sign in  

[ CAS No. 113283-94-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 113283-94-6
Chemical Structure| 113283-94-6
Structure of 113283-94-6 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 113283-94-6 ]

Related Doc. of [ 113283-94-6 ]

Alternatived Products of [ 113283-94-6 ]

Product Details of [ 113283-94-6 ]

CAS No. :113283-94-6 MDL No. :MFCD11858354
Formula : C12H18N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 222.28 Pubchem ID :-
Synonyms :

Safety of [ 113283-94-6 ]

Signal Word: Class:
Precautionary Statements: UN#:
Hazard Statements: Packing Group:

Application In Synthesis of [ 113283-94-6 ]

* 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 [ 113283-94-6 ]

[ 113283-94-6 ] Synthesis Path-Downstream   1~5

  • 2
  • [ 623-09-6 ]
  • [ 113283-94-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: aq. Na2CO3 2: DMAP / acetonitrile / 15 h / Ambient temperature 3: 98 percent / H2 / Pd/C / methanol
  • 3
  • [ 113283-94-6 ]
  • [ 62-50-0 ]
  • [ 1111628-41-1 ]
  • 4
  • [ 66-27-3 ]
  • [ 71026-66-9 ]
  • [ 113283-94-6 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In dichloromethane; at 0℃;Reflux; General Procedure for the Alkylation of Primary and Secondary Amines: Method C.The alkylating agent (10.0 mmol of <strong>[66-27-3]methyl methanesulfonate</strong> or ethyl methanesulfonate) and 10.0 mmol of TEA were added at 0 C. over a solution containing 10.0 mmol of the corresponding amine in DCM (12 mL). The resulting mixture was heated at reflux temperature for 15 h and after cooling it was diluted with 40 mL of DCM, washed with a 10% NaOH solution (2×15mL) and water (2×15 mL). The organic phase was dried over anhydrous Na2SO4, filtered and concentrated under vacuum to give a residue that was purified by silica gel column chromatography, eluting with the appropriate hexane:EtOAc mixture.
  • 5
  • [ 113283-94-6 ]
  • [ 623-09-6 ]
YieldReaction ConditionsOperation in experiment
Stage #1: N4-Boc-N1-methyl-1,4-phenylenediamine With trifluoroacetic acid In dichloromethane at 0℃; Reflux; Stage #2: With sodium hydroxide In water General Procedure for the BOC-Deprotection and Preparation of the Starting Material Amines: Method D.A solution containing 10.0 mmol of the BOC-protected compound (11, 12 or 15) in 15 mL of TFA was stirred at room temperature for 2 h. Then, the solvent was eliminated under vacuum to generate the trifluoroacetate salt. This salt was redissolved in 20 mL of an aqueous solution of NaOH (2M) and washed with DCM (3×15 mL). The organic layer was washed with water (2×10 mL), dried over anhydrous Na2SO4, filtered and concentrated to give the corresponding free amine as an oil.
Same Skeleton Products
Historical Records