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Chemical Structure| 225517-15-7 Chemical Structure| 225517-15-7

Structure of 225517-15-7

Chemical Structure| 225517-15-7

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Product Details of [ 225517-15-7 ]

CAS No. :225517-15-7
Formula : C14H19NO5
M.W : 281.30
SMILES Code : O=C(OC)[C@@H](NC(OC(C)(C)C)=O)C1=CC=C(O)C=C1
MDL No. :MFCD29077614
Boiling Point : No data available
InChI Key :HGJGPDQDXKDZTQ-NSHDSACASA-N
Pubchem ID :11380492

Safety of [ 225517-15-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 225517-15-7 ]

* 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 [ 225517-15-7 ]

[ 225517-15-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 69651-48-5 ]
  • [ 18107-18-1 ]
  • [ 225517-15-7 ]
YieldReaction ConditionsOperation in experiment
66% In methanol; hexane; benzene; at 0℃; In a 50 mL round bottomed flask was added a 1:1 mixture of benzene:methanol and N-tert-butoxycarbonyl-(S)-4-hydroxyphenylglycine (2.8 g, 11 mmol). The solution was cooled to 0 C. and a 2 M solution of trimethylsilyldiazomethane (Aldrich Chemical Co.) in hexane was added with vigorous stirring until a slight yellow color persisted. Then the reaction mixture solvents were removed under reduced pressure and the crude product was purified by flash chromatography (80/20 hexane/ethyl acetate) to give N-tert-butyloxycarbonyl-(S)-4-hydroxyphenylglycine, methyl ester (2.05 g, 7.3 mmol) (66% yield). 300 MHz 1H NMR (CDCl3): delta1.43 (s, 9H), 3.71 (s, 3H), 5.22 (br d, 1H), 5.57 (1H, br d), 5.80 (br s, 1H), (6.7 (d, 2H, J=8 Hz), 7.17 (d, 2H, J=8 Hz).
With methanol; In toluene; Preparation 15: (.S)-ferf-Butoxycarbonylamino-(4-hydroxyphenyl)acetic acid methyl ester; Trimethylsilyldiazomethane (5.40 mL, 7.62 mmol) was added dropwise to a solution of (5)-ferf-butoxycarbonylamino-(4-hydroxyphenyl)acetic acid (Preparation 14, 2.00 g, 7.48 mmol) in toluene:MeOH (4:1, 50 mL). The clear solution turned yellow and the MeOH was removed in vacuo. The remainder was diluted with EtOAc (100 mL), washed with H2O (50 mL), saturated NaHCO3 solution (50 mL) and brine (50 mL) before being dried (MgSO4), filtered and concentrated in vacuo, azeotroping several times with Et2O, to afford the title compound: RT = 2.98 min, m/z (ES+) = 282.1 [M + H]+.
 

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