5-(Trifluoromethyl)pyridine-2-carboxylic acid synthesis
- Product Name:5-(Trifluoromethyl)pyridine-2-carboxylic acid
- CAS Number:80194-69-0
- Molecular formula:C7H4F3NO2
- Molecular Weight:191.11
67-56-1
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201230-82-2
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52334-81-3
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$5.00/1g
124236-37-9
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$13.00/250mg
80194-69-0
187 suppliers
$10.00/1g
Yield:124236-37-9 79% ,80194-69-0 15%
Reaction Conditions:
with bis-triphenylphosphine-palladium(II) chloride;triethylamine;n-butyl-diphenylphosphane at 120; under 2280.15 Torr; for 3 h;Autoclave;
Steps:
2 Reference Example 2
Reference Example 2 (0150) Production Method of 5-(trifluoromethyl)pyridine-2-carboxylic acid ester (0151) A 100-mL autoclave was charged successively with 2-chloro-5-(trifluoromethyl)pyridine (24.55 g, 135.26 mmol), PdCl2(PPh3)2 (474 mg, 0.5 mol %), diphenylphosphinobutane (DPPB, 1.45 g, 2.5 mol %), triethylamine (24 mL) and methanol (50 mL). The atmosphere in the reaction system was replaced by carbon monoxide 3 times. After charging with carbon monoxide to a pressure of 3 atmospheres, the mixture in the autoclave was stirred under heating at 120° C. for 3 hours. After cooling to room temperature, water and ethyl acetate were added to the reaction mixture, and extraction was repeated about 3 times, followed by drying and concentration. The concentrate was subjected to column chromatography (from hexane: ethyl acetate=5:1 to ethyl acetate) to give a methyl ester compound (21.8 g, 79%) and a carboxylic acid compound (3.86 g, 15%).
References:
NIHON NOHYAKU CO., LTD.;YONEMURA, Ikki;MATSUO, Soichiro;SUWA, Akiyuki;YAMASHITA, Masao;OKADA, Atsushi US2016/366884, 2016, A1 Location in patent:Paragraph 0150; 0151
95727-86-9
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80194-69-0
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$10.00/1g
124-38-9
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50488-42-1
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80194-69-0
187 suppliers
$10.00/1g
124-38-9
129 suppliers
$175.00/23402
100366-75-4
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$9.00/1g
80194-69-0
187 suppliers
$10.00/1g
52334-81-3
428 suppliers
$5.00/1g
80194-69-0
187 suppliers
$10.00/1g