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CAS No. : | 98977-34-5 | MDL No. : | MFCD01862189 |
Formula : | C13H21NO5 | Boiling Point : | No data available |
Linear Structure Formula : | (CH3)3COCONC5H7OCO2CH2CH3 | InChI Key : | ABBVAMUCDQETDO-UHFFFAOYSA-N |
M.W : | 271.31 | Pubchem ID : | 6420876 |
Synonyms : |
|
Chemical Name : | 1-tert-Butyl 3-ethyl 4-oxopiperidine-1,3-dicarboxylate |
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P280-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H332-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 |
---|---|---|
81% | With potassium carbonate; In N,N-dimethyl-formamide; at 70℃; | General procedure: A 10 mL round bottom flask was charged with phenylamidinium hydrochloride (31.7 mg, 0.203 mmol), 3-carbethoxy-4-piperidone hydrochloride (50 mg, 0.184 mmol), powdered K2CO3 (63.7 mg, 0.461 mmol), and a stirbar. The flask was sealed and charged with DMF (1.23 mL) followed by allyl chloride (37.9 muL, 0.461 mmol). With vigorous stirring, the reaction mixture was heated to 70 °C for 2 h, and reaction progress was monitored by LCMS. Upon completion of the reaction, the reaction mixture was diluted with EtOAc (10 mL), and washed with sat. aq NaHCO3 (10 mL) and brine (10 mL). The combined aqueous phases were back-extracted with EtOAc (5 mL), and the combined organic phases were dried over Na2SO4, filtered, and concentrated in vacuo. The resulting residue was purified by gradient elution on silica gel (0-25percent EtOAc/hexanes) to afford the title compound. |
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