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Chemical Structure| 168297-84-5 Chemical Structure| 168297-84-5

Structure of 168297-84-5

Chemical Structure| 168297-84-5

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Product Details of [ 168297-84-5 ]

CAS No. :168297-84-5
Formula : C11H13NO2
M.W : 191.23
SMILES Code : CC1(C)OC(=O)N[C@H]1C1=CC=CC=C1
English Name :(S)-5,5-Dimethyl-4-phenyl-2-oxazolidinone
MDL No. :MFCD00274262

Safety of [ 168297-84-5 ]

Application In Synthesis of [ 168297-84-5 ]

* 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 [ 168297-84-5 ]

[ 168297-84-5 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 530-62-1 ]
  • [ 168297-77-6 ]
  • [ 168297-84-5 ]
YieldReaction ConditionsOperation in experiment
In dichloromethane
  • 2
  • [ 204851-68-3 ]
  • [ 168297-84-5 ]
  • [ 170918-42-0 ]
YieldReaction ConditionsOperation in experiment
With diphenyl phosphoryl azide; triethylamine In toluene at 80℃; for 8h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
  • 3
  • [ 33664-93-6 ]
  • [ 97-72-3 ]
  • [ 896131-91-2 ]
  • [ 168297-84-5 ]
  • [ 170918-42-0 ]
YieldReaction ConditionsOperation in experiment
With (R)-BTM; sodium sulfate; N-ethyl-N,N-diisopropylamine In chloroform at 20℃; for 12h;
  • 4
  • [ 2523432-30-4 ]
  • [ 168297-84-5 ]
  • [ 170918-42-0 ]
YieldReaction ConditionsOperation in experiment
1: 60.2 % ee 2: 60.2 % ee With 3-amino-7-dimethylamino-2-methylphenazine hydrochloride; C20H20N2O2; N-ethyl-N,N-diisopropylamine In Hexafluorobenzene at 60℃; for 12h; Irradiation; Overall yield = 40 percent; 3 Example 3 Screening of Chiral Additives: Taking the compound represented by formula I-2 as the substrate (0.2mmol), adding organic photocatalyst neutral red (0.004mmol), solvent perfluorobenzene (8mL), diisopropylethylamine (0.2mmol), chiral Additive (0.02mmol), the chiral additive is shown in Table 1 and chemical formula, and then reacted at 60 ° C under the irradiation of 5w blue LED for 12 hours, the product was separated by column chromatography, and the product yield and ee value were shown in Table 1 shown.
With 3-amino-7-dimethylamino-2-methylphenazine hydrochloride; C20H20N2O2; N-ethyl-N,N-diisopropylamine In Hexafluorobenzene at 60℃; for 12h; Irradiation; Optical yield = 60.2 percent ee; 3 Example 3 Screening of Chiral Additives: Taking the compound represented by formula I-2 as the substrate (0.2mmol), adding organic photocatalyst neutral red (0.004mmol), solvent perfluorobenzene (8mL), diisopropylethylamine (0.2mmol), chiral Additive (0.02mmol), the chiral additive is shown in Table 1 and chemical formula, and then reacted at 60 ° C under the irradiation of 5w blue LED for 12 hours, the product was separated by column chromatography, and the product yield and ee value were shown in Table 1 shown.
  • 5
  • [ 2762724-58-1 ]
  • [ 168297-84-5 ]
  • [ 170918-42-0 ]
YieldReaction ConditionsOperation in experiment
77 % ee With neutral red; N-ethyl-N,N-diisopropylamine; 2,2-bis[(4S)-4-isopropyloxazolin-2-yl]propane In Hexafluorobenzene at 40℃; for 12h; Irradiation; Overall yield = 16 percent; enantioselective reaction;
 

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