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3-(4-Methylbenzoyl)propionic acid

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3-(4-Methylbenzoyl)propionic acid manufacturers

3-(4-Methylbenzoyl)propionic acid Basic information
Product Name:3-(4-Methylbenzoyl)propionic acid
Synonyms:AKOS BB-9554;AKOS BBS-00003761;3-(4-METHYLBENZOYL)PROPIONIC ACID;3-(P-TOLUOYL)PROPIONIC ACID;4-(4-METHYLPHENYL)-4-OXOBUTYRIC ACID;4-OXO-4-P-TOLYLBUTANOIC ACID;4-OXO-4-P-TOLYL-BUTYRIC ACID;4-OXO-4-(4-TOLYL)BUTYRIC ACID
CAS:4619-20-9
MF:C11H12O3
MW:192.21
EINECS:
Product Categories:Miscellaneous;C11 to C12;Carbonyl Compounds;Carboxylic Acids
Mol File:4619-20-9.mol
3-(4-Methylbenzoyl)propionic acid Structure
3-(4-Methylbenzoyl)propionic acid Chemical Properties
Melting point 127-130 °C(lit.)
Boiling point 288.19°C (rough estimate)
density 1.1430 (rough estimate)
refractive index 1.5340 (estimate)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
pka4.57±0.17(Predicted)
color White to Almost white
Water Solubility insoluble
BRN 2099653
InChI1S/C11H12O3/c1-8-2-4-9(5-3-8)10(12)6-7-11(13)14/h2-5H,6-7H2,1H3,(H,13,14)
InChIKeyOEEUWZITKKSXAZ-UHFFFAOYSA-N
SMILESCc1ccc(cc1)C(=O)CCC(O)=O
CAS DataBase Reference4619-20-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 2915601990
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
3-(4-Methylbenzoyl)propionic acid Usage And Synthesis
Chemical PropertiesWhite to light beige crystalline powder
Uses3-(4-Methylbenzoyl)propionic acid can be used as an intermediate in agrochemical, pharmaceutical and dyestuff field
General Description4-(4-Methylphenyl)-4-oxobutyric acid is an organic building block. It is a commercial corrosion inhibitor.
Synthesis
Succinic anhydride

108-30-5

Toluene

108-88-3

3-(4-Methylbenzoyl)propionic acid

4619-20-9

The general procedure for the synthesis of 3-(4-methylbenzoyl)propionic acid from succinic anhydride and toluene was as follows: 75.7 g of succinic anhydride was dissolved in 457.5 mL of toluene. Under stirring, 220.5 g of anhydrous aluminum trichloride (AlCl3) was added in batches. The temperature of the reaction mixture was maintained in the range of 50-60 °C. After 2 hours of reaction, the completion of the reaction was monitored by thin layer chromatography (TLC). The reaction mixture was slowly added dropwise to 1250 mL of 1 mol/L ice hydrochloric acid under vigorous stirring. During the dropwise addition, milky solids were gradually precipitated. After completion of the dropwise addition, the mixture was continued to be stirred for 0.5 h, followed by filtration. The filter cake was washed sequentially with toluene and ice water and then pumped with 50 mL of ethyl acetate. The resulting solution was slowly added to 500 mL of petroleum ether to induce crystallization. After stirring for 0.5 h, the crystals were collected by filtration and dried at 40 °C for 2 h to give 144 g of Compound II (intermediate) in 99.3% yield. [Compound II intermediate] was a white solid.

References[1] Organic Letters, 2016, vol. 18, # 3, p. 504 - 507
[2] Patent: CN107628947, 2018, A. Location in patent: Paragraph 0053; 0054; 0055; 0056; 0057
[3] Russian Journal of General Chemistry, 2014, vol. 84, # 9, p. 1825 - 1829
[4] Zhurnal Obshchei Khimii, 2014, vol. 84, # 9, p. 1825 - 1829,5
[5] Molecules, 2018, vol. 23, # 3,
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