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CAS No. : | 65874-27-3 | MDL No. : | MFCD01111994 |
Formula : | C12H14O3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | DUNFNBQQWYQKFE-UHFFFAOYSA-N |
M.W : | 206.24 | Pubchem ID : | 2751588 |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
346.1 mg | A) (S)-Di-tert-butyl 2-((4-(tert-butoxycarbonyl)benzyl)amino) succinate Acetic acid (0.212 mL) was added to a mixture of <strong>[1791-13-5]L-<strong>[1791-13-5]aspartic acid di-tert-butyl ester hydrochloride</strong></strong> (418 mg), tert-butyl 4-formylbenzoate (306 mg), and THF (8 mL) at room temperature, followed by stirring at the same temperature for 1 hour. Sodium triacetoxyborohydride (786 mg) was added to the reaction mixture at room temperature, followed by stirring at the same temperature overnight. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture at 0 C., followed by extraction with ethyl acetate. The organic layer was washed with a saturated saline solution and was then dried over anhydrous magnesium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the title compound (346.1 mg). MS: [M+H]+ 436.2. |
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