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CAS No. : | 31576-51-9 | MDL No. : | MFCD09032941 |
Formula : | C5H13NO2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | QWCGXANSAOXRFE-UHFFFAOYSA-N |
M.W : | 119.16 | Pubchem ID : | 520530 |
Synonyms : |
|
Chemical Name : | 2-(2-Methoxyethoxy)ethanamine |
Signal Word: | Danger | Class: | 6.1 |
Precautionary Statements: | P210-P264-P270-P280-P301+P310+P330-P370+P378-P403+P235-P405-P501 | UN#: | 2810 |
Hazard Statements: | H227-H301 | Packing Group: | Ⅲ |
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 |
---|---|---|
880 mg | With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; In dichloromethane; ethyl acetate; N,N-dimethyl-formamide; at 20℃;Cooling with ice; | (i) 3-Ami no-5-bromo-N-(2-(2-methoxyethoxy)ethyl)benzamideA stirred mixture of <strong>[42237-85-4]3-amino-5-bromobenzoic acid</strong> (800 mg, 3.59 mmol), 2-(2- methoxyethoxy)ethanamine (856 mg, 7.18 mmol) and Et3N (1.5 mL, 10.76 mmol) in DCM (13mL) was cooled in an ice bath. T3P (50 w/w in EtOAc, 3.2 mL, 5.38 mmol) was added dropwise, the ice bath was removed and the reaction mixture allowed to warm to room temperature. DMF (2 mL) was added to aid solubility and the reaction stirred at room temperature overnight. The reaction mixture was partitioned between sat. aq. NaHCO3 (50 mL) and DCM (50 mL). The aqueous phase was back extracted with fresh DCM (50 mL).The combined organic extracts were washed with water (100 mL), brine (100 mL), dried (MgSO4), filtered and concentrated in vacuo to afford an orange oil. The crude product was purified by chromatography on silica gel (40 g column, 0-5% MeOH) to afford the sub-title compound (880 mg) as an orange oil.1H NMR (DMSO-d6) 400 MHz, O: 8.36 (t, 1H), 7.07 (t, 1H), 7.00-6.99 (m, 1H), 6.84 (t, 1H),5.57 (s, 2H), 3.53-3.48 (m, 4H), 3.44-3.42 (m, 2H), 3.35 (q, 2H), 3.23 (s, 3H). LCMS m/z 317/319 (M÷H) (ES) |
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