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Chemical Structure| 1086703-01-6 Chemical Structure| 1086703-01-6

Structure of 1086703-01-6

Chemical Structure| 1086703-01-6

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Product Details of [ 1086703-01-6 ]

CAS No. :1086703-01-6
Formula : C14H17NO5
M.W : 279.29
SMILES Code : O=C(N([C@H]1C2=CC=C(O)C=C2)COC1=O)OC(C)(C)C

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* 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 [ 1086703-01-6 ]

[ 1086703-01-6 ] Synthesis Path-Downstream   1~1

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  • [ 69651-48-5 ]
  • [ 1086703-01-6 ]
YieldReaction ConditionsOperation in experiment
36 g With toluene-4-sulfonic acid; In benzene; at 120℃;Dean-Stark; To a solution of (S)-2-((tert-butoxycarbonyl)amino)-2-(4- hydroxyphenyl)acetic acid (45 g, 0.17 mol) in dry benzene (500 mL) was added paraformaldehyde (75.6 g, 0.84 mol, 5 eq) and p-toluenesulfonic acid (1.6 g, 8.5 mmol, 0.05 eq). A Dean-Stark apparatus with an attached condenser was then fit to the top of the flask and the mixture was heated at approximately 120C until LC-MS showed the reaction was complete.The reaction was then cooled and the benzene was evaporated. The residue was taken up in ethyl acetate, washed with saturated NaHCO3 (2 x 150 mL), then dried over sodium sulfate, and filtered. The solvent was removed to give (5)-tert-butyl 4-(4-hydroxyphenyl)-5-oxooxazolidine- 3-carboxylate (36 g, 76.5%).
36 g With toluene-4-sulfonic acid; In benzene; at 120℃;Dean-Stark; To a solution of (S)-2-((tert-butoxycarbonyl)amino)-2-(4- hydroxyphenyl)acetic acid (45 g, 0.17 mol) in dry benzene (500 mL) was added paraformaldehyde (75.6 g, 0.84 mol, 5 eq) and p-toluenesulfonic acid (1.6 g, 8.5 mmol, 0.05 eq). A Dean-Stark apparatus with an attached condenser was then fit to the top of the flask and the mixture was heated at approximately 120C until LC-MS showed the reaction was complete.The reaction was then cooled and the benzene was evaporated. The residue was taken up in ethyl acetate, washed with saturated NaHCO3 (2 x 150 mL), then dried over sodium sulfate, and filtered. The solvent was removed to give (5)-tert-butyl 4-(4-hydroxyphenyl)-5-oxooxazolidine- 3-carboxylate (36 g, 76.5%).
 

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