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CAS No. : | 2457-76-3 | MDL No. : | MFCD00007772 |
Formula : | C7H6ClNO2 | Boiling Point : | - |
Linear Structure Formula : | H2NC6H3(Cl)CO2H | InChI Key : | MBDUKNCPOPMRJQ-UHFFFAOYSA-N |
M.W : | 171.58 | Pubchem ID : | 17154 |
Synonyms : |
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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 urea; sodium nitrite; In water; | Synthesis of 2-chloro-4-cyanobenzoic acid (used in the synthesis of Compound 25) To a stirred suspension of 4-amino-2-chlorobenzoic acid (10 g, supplied by Aldrich) in water (150 ml) and concentrated sulphuric acid (20 ml) at -2C was added a solution of sodium nitrite (4.8 g) in water (75 ml) at -2C. After the solid had dissolved, urea was added to destroy excess nitrous acid. The resulting solution was added to a stirred solution of copper (I) cyanide (9.0 g) and potassium cyanide (13.0 g) in water (30 ml) at 60-70C and the mixture was heated to 85-90C for 1 hour. The hot mixture was filtered. The filtrates were cooled and the product was filtered off. 1.3 g of 2-chloro-4-cyanobenzoic acid was obtained. Nuclear magnetic resonance spectrum (NMR) was as follows: 'H (ppm from TMS in (CD3)2CO, integral, number of peaks): 7.85, 1H, dd; 8.0, 1H, d; 8.05 1H, d. Mass spectrum M+1 182. |
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