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CAS No. : | 84478-75-1 | MDL No. : | MFCD02670258 |
Formula : | C6H3ClFNO3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | NAWVMCKMQMJQMF-UHFFFAOYSA-N |
M.W : | 191.54 | Pubchem ID : | 158655 |
Synonyms : |
|
Signal Word: | Danger | Class: | 9 |
Precautionary Statements: | P261-P264-P270-P272-P273-P280-P301+P312+P330-P302+P352-P305+P351+P338+P310-P333+P313-P391-P501 | UN#: | 3077 |
Hazard Statements: | H302-H315-H317-H318-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 |
---|---|---|
95.6% | With hydrogen;palladium 10% on activated carbon; In ethanol; for 4h; | Pd/C (10%, 1 g) was charged to a flask under nitrogen followed by the addition of Intermediate 10 (10 g, 51.93 mmol) dissolved in EtOH (250 mL). The reaction was stirred for approximately 4 hours under H2 (3739 ml, 155.8 mmol) and was then purged with nitrogen gas before removing the catalyst by filtration through a glass fiber pad. The filtrate was concentrated in vacuo to yield the desired product (8.08 g, 95.6%). |
platinum (IV) oxide; In ethanol; | EXAMPLE 4 Production of the aminophenol (VI) A suspension of 2-chloro-4-fluoro-5-nitrophenol (9.17 g) and platinum dioxide (500 mg) in ethanol (120 ml) was subjected to catalytic reduction with hydrogen at room temperature and atmospheric pressure until a designed amount of hydrogen was absorbed. The catalyst was removed by filtration, and the filtrate was concentrated. The residue was extracted with ether, and the ether layer was concentrated to obtain 6.6 g of 3-amino-6-chloro-4-fluorophenol. M.P., 145-146 C. (decomp.). NMR (CDCl3, D6 -DMSO), delta (ppm): 6.4 (1H, d, J=8 Hz), 6.85 (1H, d, J=11 Hz). IR numaxnujol (cm-1): 3400, 3320. | |
platinum (IV) oxide; In ethanol; | EXAMPLE 8 Production of the aminophenol (VII: X=Cl): A suspension of 2-chloro-4-fluoro-5-nitrophenol (9.17 g) and platinum dioxide (500 mg) in ethanol (120 ml) was subjected to catalytic reduction with hydrogen under room temperature and atmospheric pressure until a designed amount of hydrogen was absorbed. The catalyst was removed by filtration, and the filtrate was concentrated. The residue was extracted with ether, and the ether layer was concentrated to obtain 6.6 g of 3-amino-6-chloro-4-fluorophenol. M.P., 145-146 C. (decomp.). NMR (CDCl3, D6 -DMSO) delta(ppm): 6.4 (1H, d, J=8 Hz), 6.85 (1H, d, J=11 Hz). IR numaxnujol (cm-1): 3400, 3320. |
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