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[ CAS No. 120157-94-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 120157-94-0
Chemical Structure| 120157-94-0
Structure of 120157-94-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 120157-94-0 ]

CAS No. :120157-94-0 MDL No. :MFCD21105772
Formula : C13H19NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 237.30 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 120157-94-0 ]

* 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 [ 120157-94-0 ]

[ 120157-94-0 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 41840-28-2 ]
  • [ 2393-23-9 ]
  • [ 120157-94-0 ]
YieldReaction ConditionsOperation in experiment
92% With triethylamine In 1,4-dioxane; water for 6h; Ambient temperature;
  • 2
  • [ 60421-23-0 ]
  • [ 120157-94-0 ]
  • [ 109-52-4 ]
  • 2-butyl-3-(4-methoxy-benzyl)-1,3-diaza-spiro[4.4]non-1-en-4-one [ No CAS ]
  • 3
  • [ 24424-99-5 ]
  • [ 2393-23-9 ]
  • [ 120157-94-0 ]
YieldReaction ConditionsOperation in experiment
100% With triethylamine In dichloromethane at 0 - 20℃;
98% In water at 80℃; for 0.0833333h; Microwave irradiation; Green chemistry; chemoselective reaction;
95% With choline chloride; urea at 50℃; Green chemistry; General procedure General procedure: A dried test tube, equipped with a magnetic stir bar, wascharged with 0.5 cm3 DES, amine derivatives(0.5 mmol), and Boc2O (0.5 mmol) and the mixture washeated at 50 C until the reaction was complete (monitoredby TLC and IR). After this time, 5 cm3 water wasadded and in the most cases a white solid was obtained.The solid product was collected by filtration and washedsuccessively with water and recrystallized from ethanolto get the pure final product [51-60]. The viscousproducts extracted with ethyl acetate and were purifiedby column chromatography, using ethyl acetate-petroleumether.
93% With pyridinium trifluroacetate In neat (no solvent) at 20℃; for 0.05h; Green chemistry; General procedure for the N-Boc protection of amines General procedure: To a magnetically stirred mixture of amine (1mmol) and (Boc)2O (1mmol) a catalytic amount of ionic liquid (0.2mmol) was added under solvent-free conditions at room temperature for the specified period of time. The progress of the reaction was monitored by TLC and GC-MS. The mixture extraction was carried out using ethyl acetate (2×5mL). The organic layer was washed with water (2×10mL) and dried over anhydrous Na2SO4. The solvent was evaporated under vacuum to yield highly pure N-Boc derivatives. In some cases, the purification was done by column chromatography using silica gel (60-120) by hexane-ethyl acetate as eluent to get a pure product.

  • 4
  • [ 623-12-1 ]
  • [ 1314538-55-0 ]
  • [ 120157-94-0 ]
  • 5
  • [ 1314538-55-0 ]
  • [ 19013-30-0 ]
  • [ 120157-94-0 ]
  • 6
  • [ 1314538-55-0 ]
  • [ 1138-62-1 ]
  • [ 120157-94-0 ]
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