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CAS No. : | 107960-02-1 | MDL No. : | |
Formula : | C7H5Cl4NO5 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | - |
M.W : | 324.93 | Pubchem ID : | - |
Synonyms : |
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Signal Word: | Class: | ||
Precautionary Statements: | UN#: | ||
Hazard Statements: | Packing Group: |
* 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 |
---|---|---|
94% | With 4-methyl-morpholine In tetrahydrofuran; ethyl acetate; Petroleum ether | EXAMPLE 11: PREPARATION OF N-SUCCINIMIDYL N-TERT-BUTYLOXYCARBONYL-L-ALANINATE 0.95 g (5 mmol) of N-tert-butyloxycarbonyl-L-alanine and 0.66 ml (5.5 mmol) of N-methylmorpholine are dissolved in 6 ml of THF, and 1.8 g (5.5 mmol) of N-succinimidyl 1,2,2,2-tetrachloroethyl carbonate is added in a single portion. The mixture is stirred for two hours at 20° C. Approximately 25 ml of ethyl acetate are added and the organic phase is washed rapidly with N HCl solution, then with potassium bicarbonate solution and finally twice with water. The organic phase is dried over magnesium sulphate and evaporated. The residue is crystallized in an ethyl acetate/petroleum ether mixture and 1.25 g (Y=87percent) of white crystals are obtained. Evaporation of the mother liquors and crystallisation enables a further 0.1 g to be recovered, and this brings the yield to 94percent. M.p. (melting point)=158° C. [α]D20 =50.7 (c=2, dioxane) |