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CAS No. : | 253787-45-0 | MDL No. : | MFCD12963565 |
Formula : | C11H8BrNO2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | CSGDGTYOZTXOBR-UHFFFAOYSA-N |
M.W : | 266.09 | Pubchem ID : | 46835721 |
Synonyms : |
|
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 |
---|---|---|
85% | A solution of <strong>[2840-29-1]3-amino-4-bromobenzoic acid</strong> (3.6 g, 17 mmol), glycerol (2.4 mL, 33 mmol), and 3-nitrobenzenesulfonic acid sodium salt (11 g, 50 mmol) in 75% H2SO4 (aq.) (40 mL) was stirred at 100 C. for 2 h and 140 C. for 1 h. The reaction mixture was cooled to rt and MeOH (40 mL) was added. The reaction was stirred at 60 C. After 18 h, the mixture was cooled to rt, poured into ice water and made basic with 12 M NH4OH (aq.). EtOAc was added and the solution was filtered. The layers were separated and the aqueous layer was extracted with EtOAc (2*). The combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated. The crude product was purified by flash column chromatography (120 g silica gel cartridge; A=Hex, B=EtOAc; 30 min grad.; 0% B to 70% B; flow rate=80 mL/min). The pure fractions were combined, concentrated and dried in vacuo to provide the title compound (3.8 g, 14 mmol, 85% yield) as a white solid. 1H NMR (500 MHz, CHLOROFORM-d) delta 9.48-9.35 (m, 1H), 9.10 (dd, J=3.9, 1.7 Hz, 1H), 8.17-8.05 (m, 2H), 7.60 (dd, J=8.8, 4.1 Hz, 1H), 4.02 (s, 3H). MS (ESI) 265.8, 267.8 (M+H). |
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