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CAS No. : | 7524-50-7 | MDL No. : | MFCD00012489 |
Formula : | C10H14ClNO2 | Boiling Point : | - |
Linear Structure Formula : | [H3NCH(CH2C6H5)C(O)OCH3]Cl | InChI Key : | SWVMLNPDTIFDDY-FVGYRXGTSA-N |
M.W : | 215.68 | Pubchem ID : | 75736 |
Synonyms : |
|
Chemical Name : | H-Phe-OMe.HCl |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
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 |
---|---|---|
General procedure: To a solution of N,N'-carbonyldiimidazole (CDI, 1.64g, 10.1mmol) in DMF (8mL) and acetonitrile (40mL) was added l-phenylalanine methyl ester hydrochloride (2.0g, 9.3mmol) in portions. The solution was stirred at room temperature for 2h. Benzylamine (1g, 9.3mmol) was then added, followed by the addition of triethylamine (1.72mL, 18.6mmol), and the aggregation system began to become clear. The reaction mixture was stirred at room temperature for 24h until completion as monitored by TLC, and then concentrated under reduced pressure. The residue was dissolved in ethyl acetate (50mL) and washed with brine (50mL×3), dried over anhydrous Na2SO4 and concentrated in vacuo. The crude material was recrystallized from ethyl acetate to afford the product I-1a as a white solid (1.22g, 43% yield); |
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