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CAS No. : | 2386-37-0 | MDL No. : | MFCD00030381 |
Formula : | C13H19NO4 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | KKBICYRCYZAPRF-UHFFFAOYSA-N |
M.W : | 253.29 | Pubchem ID : | 291754 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-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 |
---|---|---|
77% | With sodium; at 190℃;Heating / reflux; | c) Preparation of the Compound of Formula (4): A 2.5 l Keller round-bottomed flask equipped with a reflux condenser/distillation head, a thermometer, a dropping funnel and an argon conduit is loaded with a solution of compound (5) (95.00 g, 0.38 mol) in benzyl alcohol (685 ml) and heated to 120 C., which results in the azeotropic removal of minor amounts of water. The mixture is then heated to 190 C. The dropping funnel is loaded with a separately prepared solution of sodium (3 g) in benzyl alcohol (70 ml). This solution is added in 5 ml portions, which results in a vigorous reflux of the reaction mixture. The resulting methanol and ethanol are removed by semi-continuous distillation. The conversion is followed by HPLC. The reaction mixture is cooled to 150 C. and then transferred into a mixture of methanol (0.85 l), water (0.54 l) and acetic acid (10 ml). At 30 C., crystallization takes place rapidly. The mixture is stirred again at ambient temperature for 1 h. The product is isolated by filtration. The product is dried under reduced pressure, to give the compound (4) (113.30 g, 77%) in the form of an off-white solid.1H NMR (300 MHz, CDCl3): 2.16 (s, CH3), 2.27 (s, CH3), 2.47 (t, CH2), 2.71 (t, CH2), 4.70 (s, CH3), 5.08 (s, CH2), 5.28 (s, CH2), 7.40 (m, 10H), 8.60 (broad singlet, NH2). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
49% | With sodium hydroxide; water; for 1h;Heating / reflux; | <strong>[2386-37-0]4-(2-Methoxycarbonyl-ethyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester</strong> (Aldrich, 228 g, 0.9 mol) and 720 mL of 5 N sodium hydroxide were refluxed for one hour. Thin layer chromatography showed the hydrolysis to be complete. The stirred mixture was cooled to 50 C. and hydrochloric acid (10 N, 390 mL) was slowly added to give a pH of 2-3. The oil which separated solidified. The mixture was stirred and cooled to 4 C. The solids were collected by vacuum filtration, washed thoroughly with water and dried under vacuum at 40 C. to give 65.7 g (49% yield) of 3-(2,4-dimethyl-1H-pyrrol-3-yl)-propionic acid as a reddish solid. |
49% | [0184] <strong>[2386-37-0]4-(2-Methoxycarbonyl-ethyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester</strong> (Aldrich, 228 g, 0.9 mol) and 720 mL of 5 N sodium hydroxide were refluxed for one hour. Thin layer chromatography showed the hydrolysis to be complete. The stirred mixture was cooled to 50 C. and hydrochloric acid (10 N, 390 mL) was slowly added to give a pH of 2-3. The oil which separated solidified. The mixture was stirred and cooled to 4 C. The solids were collected by vacuum filtration, washed thoroughly with water and dried under vacuum at 40 C. to give 65.7 g (49% yield) of 3-(2,4-dimethyl-1H-pyrrol-3-yl)-propionic acid as a reddish solid. |
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