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CAS No. : | 38275-57-9 | MDL No. : | MFCD02940446 |
Formula : | C5H2BrN3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | VPQICCOHFSGBMA-UHFFFAOYSA-N |
M.W : | 183.99 | Pubchem ID : | 686546 |
Synonyms : |
|
Signal Word: | Danger | Class: | 9 |
Precautionary Statements: | P273-P280-P301+P312+P330-P302+P352+P312-P304+P340+P312-P305+P351+P338+P310 | UN#: | 3077 |
Hazard Statements: | H302+H312+H332-H315-H318-H335-H410 | 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 |
---|---|---|
61% | at -78℃; for 3.5 h; | 1-(5-Bromopyrimidin-2-yl)ethanone To a solution of 5-bromopyrimidine-2-carbonitrile (221 mg, 1.2 mmol) in THF (10 ml) was added methylmagnesium bromide (3.0 ml, 4.20 mmol, 1.4 molar, THF) at -78° C. under nitrogen. The solution was stirred at -78° C. for 3.5 hours, and then quenched with satd aq NH4Cl, and extracted with EtOAc. The combined organic layer was dried over anhydrous Na2SO4 and concentrated. The reaction was purified by column chromatography on silica gel (petroleum ether: EtOAc=1:0 to 0:1) to afford 1-(5-bromopyrimidin-2-yl)ethanone (1.55 mg, 61percent yield). 1H NMR (CDCl3 500 MHz): δ 9.00 (s, 2H), 2.80 (s, 3H). |
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