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CAS No. : | 19962-06-2 | MDL No. : | MFCD06798070 |
Formula : | C11H15NO3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | HJQNVUQTARSZDK-UHFFFAOYSA-N |
M.W : | 209.24 | Pubchem ID : | 312485 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P280 | UN#: | |
Hazard Statements: | H317 | 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 |
---|---|---|
93% | With caesium carbonate; In DMF (N,N-dimethyl-formamide); at 20℃; for 5h; | 868 mg (4.763 MMOL) 6-CHLORO-PYRIMIDINE-4-CARBOXYLIC acid methyl ester are suspended in 10 ml of DMF together with 1 g (4.763 MMOL) (3- Hydroxy-phenyl)-carbamic acid, ter-butyl ester (S. J. Gould, R. L. Eisenberg, J. Org. Chem. 56 (23), 1991, 6666) and 1.54 g (4. 763 MMOL) cesium carbonate and stirred for 5 H at room temperature. The reaction mixture is poured onto ice and extracted several times with ethyl acetate. The combined organic phases are washed with water, dried over NA2SO4, filtered and evaporated. Yield : 1.58 g (93 %) brown oil |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
78.8% | With potassium hydroxide; In acetonitrile; at 40℃; for 2h; | Dissolve 3- (tert-butoxycarbonyl) aminophenol (1.05g, 5.0mmol) in acetonitrile (10mL), add KOH (351mg, 6.25mmol), stir to 40 C, and add 3-chloro-4-fluoronitro Benzene (878 mg, 5.0 mmol) was reacted at 40 C for 2 h. The starting material disappeared. It was concentrated, EA (25 mL) was added, and water (20 mL × 2) was extracted. The organic phase was combined with anhydrous magnesium sulfate and dried, and column chromatography (P / E = 40: 1) gave 1.437 g of a colorless oil with a yield of 78.8%. |
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