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Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate

CAS No.
769195-26-8
Chemical Name:
Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate
Synonyms
RETAG-003;Sitagliptin-10;Sitagliptin Impurity 55;Sitagliptin EP Impurity 17;3-oxo-4-(2,4,5-trifluorophenyl;Methyl 3-oxo-4-(2,4,5-trifluorophenyl);Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)bu;Methyl 2,4,5-trifluoro-b-oxo-benzenebutanoate;Methyl 3-oxo-4-(2,4,5-trifluorophenyl)butanoate;Benzenebutanoicacid,2,4,5-trifluoro-b-oxo-,Methylester
CBNumber:
CB01010402
Molecular Formula:
C11H9F3O3
Molecular Weight:
246.19
MDL Number:
MFCD09833197
MOL File:
769195-26-8.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:52
Product description Number Pack Size Price
Methyl3-Oxo-4-(2,4,5-trifluorophenyl)butanoate M320785 1g $60
Methyl3-Oxo-4-(2,4,5-trifluorophenyl)butanoate M320785 5g $110
METHYL 3-OXO-4-(2,4,5-TRIFLUOROPHENYL)BUTANOATE 95.00% HCH0037407 5G $909.56
Methyl3-Oxo-4-(2,4,5-trifluorophenyl)butanoate 60177 100g $950
Methyl3-oxo-4-(2,4,5-trifluorophenyl)butanoate Z1749 1g $104
More product size

Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate Properties

Melting point 40-41 °C
Boiling point 273.3±35.0 °C(Predicted)
Density 1.330±0.06 g/cm3(Predicted)
refractive index 1.469
Flash point 115.5±20.8 °C
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
pka 9.95±0.46(Predicted)
form Solid
color Pale Yellow to Light Yellow
InChI InChI=1S/C11H9F3O3/c1-17-11(16)4-7(15)2-6-3-9(13)10(14)5-8(6)12/h3,5H,2,4H2,1H3
InChIKey XDQLWVSUKUDAEO-UHFFFAOYSA-N
SMILES C(C1C=C(F)C(F)=CC=1F)C(=O)CC(=O)OC

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H301+H311-H315-H319
Precautionary statements  P501-P270-P264-P280-P337+P313-P305+P351+P338-P361+P364-P332+P313-P301+P310+P330-P302+P352+P312-P405
HS Code  2918300090

Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC M320785 Methyl3-Oxo-4-(2,4,5-trifluorophenyl)butanoate 769195-26-8 1g $60 2021-12-16 Buy
TRC M320785 Methyl3-Oxo-4-(2,4,5-trifluorophenyl)butanoate 769195-26-8 5g $110 2021-12-16 Buy
American Custom Chemicals Corporation HCH0037407 METHYL 3-OXO-4-(2,4,5-TRIFLUOROPHENYL)BUTANOATE 95.00% 769195-26-8 5G $909.56 2021-12-16 Buy
Medical Isotopes, Inc. 60177 Methyl3-Oxo-4-(2,4,5-trifluorophenyl)butanoate 769195-26-8 100g $950 2021-12-16 Buy
AK Scientific Z1749 Methyl3-oxo-4-(2,4,5-trifluorophenyl)butanoate 769195-26-8 1g $104 2021-12-16 Buy
Product number Packaging Price Buy
M320785 1g $60 Buy
M320785 5g $110 Buy
HCH0037407 5G $909.56 Buy
60177 100g $950 Buy
Z1749 1g $104 Buy

Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate Chemical Properties,Uses,Production

Chemical Properties

Off-white solid

Uses

Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate is a useful synthetic intermediate in the synthesis of Sitagliptin (S491000); a trizolopyrazine dipeptidyl peptidase (DPP) IV inhibitor for the treatment of type II diabetes.

Preparation

The preparation of methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate is as follows:Stage 1: (2,4,5-trifluorophenyl)acetic acid With 1,1'-carbonyldiimidazole In acetonitrile for 3.5h;Stage 2: monomethyl monopotassium malonate With triethylamine; magnesium chloride In acetonitrile at 50℃; for 8h;Stage 3: In acetonitrile at 30℃; for 26h.

Synthesis

Potassium 3-methoxy-3-oxopropanoate

38330-80-2

2,4,5-Trifluorophenylacetic acid

209995-38-0

Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate

769195-26-8

Step-1: Preparation of methyl 4-(2,4,5-trifluorophenyl)-3-oxobutanoate (formula III) Potassium monomethylmalonic acid salt (MMMKS; 122.8 g), triethylamine (264 mL) and acetonitrile (1200 mL) were added to a 3 L round bottom flask (RBF), the unit was equipped with a condenser, nitrogen inlet, thermometer casing and overhead stirrer. MgCl2 (65.2 g) was added in batches for 15-20 min at 30 °C, followed by stirring the mixture for 10 min. The reaction mixture was heated to 50 °C at the same temperature and maintained for 8 hours. Upon completion of the reaction, the mixture was cooled to 30 °C and labeled as Part A. To another 2 L RBF, 1,1'-carbonyldiimidazole (CDI) (110 g) and acetonitrile (250 mL) were added to a unit equipped with a nitrogen inlet, thermometer casing, addition funnel and overhead stirrer. A solution of 2,4,5-trifluorophenylacetic acid (100 g) in acetonitrile (600 mL) was slowly added dropwise at 30 °C for 30 min, followed by stirring of the reaction mixture at 30 °C for 3 h. The reaction mixture was labeled as part B. The reaction mixture was then stirred for 2 h at 30 °C for 2 min. The part B solution was added dropwise to the part A slurry over 2 h at 30 °C and the mixture was stirred. The progress of the reaction was monitored by TLC (mobile phase: n-hexane:ethyl acetate = 50:50).After 12 h, TLC analysis showed less than 5% unreacted feedstock. The reaction mixture was concentrated under reduced pressure at 50-55°C to obtain a thick slurry. Water (1000 mL) was added to the slurry and cooled to 10-15 °C before continuing to concentrate. HCl (220.6 mL) was added slowly at less than 20°C. MTBE (700 mL) was added and the mixture was stirred for 30 minutes. The layers were separated and the aqueous layer was extracted with MTBE (200 mL). The organic layers were combined and washed sequentially with 7% aqueous NaHCO3 (400 mL) and brine (200 mL). The organic layer was dried with sodium sulfate and concentrated under vacuum at 50 °C to give an oil (120 g). The resulting oily substance was diluted with isopropanol (400 mL) and cooled to 20 °C. Water (800 mL) was slowly added at 18-20 °C for 4 hours. The slurry was then stirred for 4 hours and filtered. The filter cake was washed with water (100 mL) and dried to give the free solid of the title product. Yield: 115 g (83%); Melting point: 37-39 °C; HPLC purity: >95%. 1H NMR (CDCl3): δ 3.64 (s, 3H), 3.75 (s, 2H), 3.85 (s, 2H), 6.88-7.11 (m, 2H). MS: 247 [M+H]+.

References

[1] Tetrahedron Asymmetry, 2006, vol. 17, # 2, p. 205 - 209
[2] Patent: WO2012/25944, 2012, A2. Location in patent: Page/Page column 29-30
[3] Patent: US2013/158265, 2013, A1. Location in patent: Paragraph 0156; 0157; 0158; 0159; 0160

38330-80-2
209995-38-0
769195-26-8
Synthesis of Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate from Potassium 3-methoxy-3-oxopropanoate and 2,4,5-Trifluorophenylacetic acid
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View Lastest Price from Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
	Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate pictures 2025-09-25 Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate
769195-26-8
US $5.00-0.10 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
3-OXO-4-(2,4,5-TRIFLUORO-PHENYL)-BUTYRIC ACID METHYL ESTER pictures 2023-05-31 3-OXO-4-(2,4,5-TRIFLUORO-PHENYL)-BUTYRIC ACID METHYL ESTER
769195-26-8
US $0.00 / Kg 1Kg 99.0% up 50 tons per month Xinxiang Hongqi District Houyuan Trading Co.,Ltd
Methyl 3-oxo-4-(2,4,5-trifluorophenyl)butanoate pictures 2023-05-31 Methyl 3-oxo-4-(2,4,5-trifluorophenyl)butanoate
769195-26-8
US $0.00 / Kg 1Kg 99.0% up 50 tons per month Xinxiang Hongqi District Houyuan Trading Co.,Ltd

Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)butanoate Spectrum

3-OXO-4-(2,4,5-TRIFLUORO-PHENYL)-BUTYRIC ACID METHYL ESTER 2,4,5-TRIFLUORO-BETA-OXO-BENZENEBUTANOIC ACID METHYL ESTER Methyl 3-oxo-4-(2,4,5-trifluorophenyl)butanoate 4-(2,4,5 )triflorophenyl 3-oxobutanoic acid, Methy ester 3-oxo-4-(2,4,5-trifluorophenyl Benzenebutanoicacid,2,4,5-trifluoro-b-oxo-,Methylester Methyl 2,4,5-trifluoro-b-oxo-benzenebutanoate Methyl 3-oxo-4-(2,4,5-trifluorophenyl) RETAG-003 Sitagliptin Impurity 55 4-(2,4,5-trifluoro-phenyl)-3-oxo-butyric acid methyl ester Sitagliptin-10 3-oxo-4-(2,4,5-trifluorophenyl)butanoic acid methyl ester Benzenebutanoic acid, 2,4,5-trifluoro-β-oxo-, methyl ester Sitagliptin EP Impurity 17 2,4,5-Trifluoro-β-oxo-benzenebutanoic Acid Methyl Ester ethyl (S)-3-acetamido-4-(2,4,5-trifluorophenyl)butanoate Methyl 3-Oxo-4-(2,4,5-trifluorophenyl)bu 769195-26-8