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Chemical Structure| 23204-70-8 Chemical Structure| 23204-70-8

Structure of 23204-70-8

Chemical Structure| 23204-70-8

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Product Details of [ 23204-70-8 ]

CAS No. :23204-70-8
Formula : C15H13NO2
M.W : 239.27
SMILES Code : [H][C@]1(NC(=O)O[C@]1([H])C1=CC=CC=C1)C1=CC=CC=C1
MDL No. :MFCD00799526

Safety of [ 23204-70-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 23204-70-8 ]

* 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 [ 23204-70-8 ]

[ 23204-70-8 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 23204-70-8 ]
  • [ 16957-70-3 ]
  • [ 866108-41-0 ]
YieldReaction ConditionsOperation in experiment
83% To a solution of (E) -2-methyl-2-pentenoic acid (5.3 g, 47 mmol) in 250 mL of THF at 0°C was added 16.3 mL (117 mmol) of triethylamine, then 5.8 mL (47 mmol) of pivaloyl chloride resulting in a thick suspension. The mixture was stirred for 1 hour at 0°C at which time 2.0 g (47 mmol) of lithium chloride was added in one portion, followed by 10 g (42 mmol) of (4S, 5R)-4, 5-diphenyl-2-oxazolidinone in four batches. Stirring was maintained throughout the solid additions. The reaction mixture was stirred for 1 hour at 0°C, and for 1 hour at ambient temperature, and was vacuum filtered through a coarse frit and concentrated. The residue was partitioned between EtOAc/water, and the organics were dried over MgS04 and concentrated. To the residue was added 200 mL of MTBE and the mixture was warmed cautiously with swirling. The warm slurry was filtered to provide 13.0 g (83percent yield) of the titled compound as a colorless solid : 1H NMR (CDC13) o7. 12 (m, 3H), 7. 08 (m, 3H), 6.93 (m, 2H), 6.86 (m, 2H), 6.14 (m, 1H), 5.90 (d, J = 7. 8 Hz, 1H), 5.69 (d, J = 7.8 Hz, 1H), 2.23 (pent, J = 7.6 Hz, 2H), 1.92 (s, 3H), 1.07 (t, J = 7.6 Hz, 3H). The titled acylated oxazolidinone may be used in the next step instead of (S)-3- ( (E)-2-Methyl-pent-2-enoyl)-4-phenyl-oxazolidin-2-one.
83% To a solution of (E)-2-methyl-2-pentenoic acid (5.3 g, 47 mmol) in 250 mL of THE at 0°C was added 16.3 mL (117 mmol) of triethylamine, then 5.8 mL (47 '?(at)9(at)^'^-) cf r""<(at)vt:1(at)''''''''t,(at) as No.asail'=I=g INo. ; {(at)i(at):(at)(at).I (at)(at) .(at)(at)(at)(at)(at):,...,.."1":' '"(at)3 7a :;.as (at):':'3(at) ...l(at).V- '-r=r (at))J. -.:..J....JY. (at)-..v........'Y -""(at)(at)'(at)'-'H, .." v... u.""u.(at) '::.."-...l."No.,-",(at),(at).,,-,,,,......JI-......(at)....(at) ....J .;.;as aizl*t 1: '(at)::-l(at) .: (at)-_:::-:(at) :(at)(at).t ::°,::: t(at)(at) ..-,(at).(at)(at)::;:,": ?o:' :<:1 :(at)(at)(at):;(at),. (at)(at)(at):(at)(at):(at)(at) :;(at)(at)(at)=(at):iR (at)y'-',;E:5 E(at)i(at)-;: one portion, followed by 10 g (42 mmol) of (4S,5R)-4,5-diphenyl-2-oxazolidinone in four batches. Stirring was maintained throughout the solid additions. The reaction mixture was stirred for 1 hour at 0°C, and for 1 hour at ambient temperature, and was vacuum filtered through a coarse frit and concentrated. The residue was partitioned between EtOAc/water, and the organics were dried over MgS04 and concentrated. To the residue was added 200 mL of MTBE and the mixture was warmed cautiously with swirling. The warm slurry was filtered to provide 13.0 g (83percent yield) of the titled compound as a colorless solid: 1H NMR (CDCI3) 8 7.12 (m, 3H), 7.08 (m, 3H), 6.93 (m, 2H), 6.86 (m, 2H), 6.14 (m, 1 H), 5.90 (d, J = 7.8 Hz, 1 H), 5.69 (d, J = 7.8 Hz, 1 H), 2.23 (pent, J = 7.6 Hz, 2H), 1.92 (s, 3H), 1.07 (t, J= 7.6 Hz, 3H). The titled acylated oxazolidinone may be used in the next step instead of (S)-3-((E)-2-Methyl-pent-2-enoyl)-4-phenyl-oxazolidin-2- one.
83% To a solution of (E) -2-methyl-2-pentenoic acid (5.3 g, 47 mmol) in 250 mL of THF at 0°C was added 16.3 mL (117 mmol) of triethylamine, then 5.8 mL (47 mmol) of pivaloyl chloride resulting in a thick suspension. The mixture was stirred for 1 hour at 0°C at which time 2.0 g (47 mmol) of lithium chloride was added in one portion, followed by 10 g (42 mmol) of (4S, 5R)-4,5-diphenyl-2-oxazolidinone in four batches. Stirring was maintained throughout the solid additions. The reaction mixture was stirred for 1 hour at 0°C, and for 1 hour at ambient temperature, and was vacuum filtered through a coarse frit and concentrated. The residue was partitioned between EtOAc/water, and the organics were dried over MgS04 and concentrated. To the residue was added 200 mL of MTBE and the mixture was warmed cautiously with swirling. The warm slurry was filtered to provide 13.0 g (83percent yield) of the title compound as a colorless solid: 1H NMR (CDCl3) No. 7.12 (m, 3H), 7.08 (m, 3H), 6.93 (m, 2H), 6.86 (m, 2H), 6.14 (m, 1 H), 5.90 (d, J = 7.8 Hz, 1 H), 5.69 (d, J = 7.8 Hz, 1H), 2.23 (pent, J= 7.6 Hz, 2H), 1.92 (s, 3H), 1.07 (t, J= 7.6 Hz, 3H).
 

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