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CAS No. : | 19337-97-4 | MDL No. : | MFCD00006410 |
Formula : | C8H7NO2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | VUVORVXMOLQFMO-ONEGZZNKSA-N |
M.W : | 149.15 | Pubchem ID : | 776396 |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | 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 |
---|---|---|
With 4-methyl-morpholine; sodium borohydrid; isobutyl chloroformate; In 1,2-dimethoxyethane; water; | PREPARATION 5 Isobutyl chloroformate (4.4 ml) was added dropwise to a suspension of (E)-3-(3-pyridyl)acrylic acid (5.0 g) and N-methylmorpholine (4.05 ml) in 1,2-dimethoxyethane (50 ml) under -18° C. After being stirred at the same temperature for 0.5 hour, a solution of sodium borohydride (1.86 g) in water (10 ml) was added to the mixture all at once. The resulting mixture was poured into water and extracted with ethyl acetate. The extract was washed with brine and dried over magnesium sulfate, and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixed solvent of hexane and ethyl acetate as eluent. The fractions containing the objective compound were collected and evaporated under reduced pressure to give (E)-3-(3-pyridyl)-2-propen-1-ol (1.0 g) as an oil. NMR (CDCl3, delta): 4.40 (2H, d, J=4.0Hz), 6.52 (1H, dt, J=4.0, 16.1Hz, trans), 6.65 (1H, d, J=16.1Hz, trans), 7.45 (1H, dd, J=5.6, 8.0Hz), 7.89 (1H, d, J=8.0Hz), 8.44 (1H, d, J=15.6Hz), 8.58 (1H, s) |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
palladium on activated carbon; In N-methyl-acetamide; methanol; | Reference Example 12 Preparation of 3-(3-pyridyl)propionic acid: A mixture of 5.0 g of 3-(3-pyridyl)acrylic acid, 0.4 g of 10% palladium on activated carbon, 150 ml of methanol, and 50 ml of dimethylformamide is hydrogenated at room temperature and atmospheric pressure. After removal of the catalyst by filtration, the filtrate is concentrated to give 5.1 g of the title compound. 3-(6-Methyl-3-pyridyl)propionic acid is prepared in substantially the same manner as in Reference Example 12, using the corresponding starting materials. |
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