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CAS No. : | 380430-68-2 | MDL No. : | MFCD03411945 |
Formula : | C11H16BNO4 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | CWLNHPXWZRALFS-UHFFFAOYSA-N |
M.W : | 237.06 | Pubchem ID : | 2773228 |
Synonyms : |
|
Chemical Name : | (3-((tert-Butoxycarbonyl)amino)phenyl)boronic acid |
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 |
---|---|---|
With sodium carbonate;tetrakis(triphenylphosphine) palladium(0); In 1,2-dimethoxyethane; water; for 2.0h;Inert atmosphere; Reflux; | Reference Example 2b; Water (0.6 mL), sodium carbonate (0.16 g), 3-(tert-butoxycarbonylamino)phenylboronic acid (0.14 g), and tetrakis(triphenylphosphine)palladium(0) (29 mg) were added to an ethylene glycol dimethyl ether (2.0 mL) solution of <strong>[890315-72-7]tert-butyl 4-bromo-2-nitrobenzoate</strong> (0.15 g), followed by heating to reflux under a nitrogen atmosphere for 2 hours. The reaction mixture was cooled to room temperature, and then ethyl acetate and a saturated aqueous solution of sodium bicarbonate were added thereto. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 95-91% hexane/ethyl acetate] to obtain 0.17 g of tert-butyl 4-(3-(tert-butoxycarbonylamino)phenyl)-2-nitrobenzoate as a light yellow solid.1H-NMR (CDCl3) delta: 1.54 (9H, s), 1.58 (9H, s), 6.55-6.63 (1H, broad), 7.24-7.28 (1H, m), 7.33 (1H, d, J=8.6 Hz), 7.39 (1H, d, J=7.8 Hz), 7.74 (1H, s), 7.80 (1H, d, J=8.1 Hz), 7.84 (1H, dd, J=7.9, 1.6 Hz), 7.99 (1H, d, J=1.7 Hz). |
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