Ethyl (3-fluorobenzoyl)acetate
Ethyl (3-fluorobenzoyl)acetate Basic information
- Product Name:
- Ethyl (3-fluorobenzoyl)acetate
- Synonyms:
-
- 3-(3-FLUORO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER
- ETHYL 3-(3-FLUOROPHENYL)-3-OXOPROPANOATE
- ETHYL (3-FLUOROBENZOYL)ACETATE
- (m-Fluorobenzoyl)acetic acid ethyl ester
- 3-(3-Fluorophenyl)-3-oxopropanoic acid ethyl ester
- Ethyl 2-3-fluorobenzoylacetate
- Ethyl 3-fluoro-β-oxobenzenepropanoate
- Ethyl m-fluorobenzoyl acetate
- CAS:
- 33166-77-7
- MF:
- C11H11FO3
- MW:
- 210.2
- Product Categories:
-
- C10 to C11
- Carbonyl Compounds
- Esters
- Mol File:
- 33166-77-7.mol
Ethyl (3-fluorobenzoyl)acetate Chemical Properties
- Boiling point:
- 262-263 °C(lit.)
- Density
- 1.166 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.5172(lit.)
- Flash point:
- >230 °F
- storage temp.
- Sealed in dry,Room Temperature
- form
- Liquid
- pka
- 10.10±0.46(Predicted)
- color
- Colorless to orange
- CAS DataBase Reference
- 33166-77-7(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
Ethyl (3-fluorobenzoyl)acetate Usage And Synthesis
Uses
Reactant for:
- Preparation of biologically active molecules
Synthesis
To a stirring suspension of NaH and CO(OEt)2 in toluene was added dropwise a solution of substituted acetophenone in toluene under reflux. The mixture was allowed to reflux and was stirred for 20 min after the addition was complete. When cooled to room temperature, the mixture was acidified with glacial HOAc. After ice-cold water was added, the mixture was extracted with toluene. The extract was then dried over anhydrous MgS04. After the toluene was evaporated in vacuo to give the corresponding substituted Ethyl (3-fluorobenzoyl)acetate.
References
[1] Bioorganic and Medicinal Chemistry, 2013, vol. 21, # 17, p. 5064 - 5075
[2] Patent: WO2014/179401, 2014, A1. Location in patent: Page/Page column 9; 14; 15
[3] Journal of Medicinal Chemistry, 1997, vol. 40, # 19, p. 3049 - 3056
[4] European Journal of Organic Chemistry, 2015, vol. 2015, # 17, p. 3656 - 3660
[5] Chemical Communications, 2017, vol. 53, # 58, p. 8136 - 8139
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