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Chemical Structure| 227184-02-3 Chemical Structure| 227184-02-3

Structure of 227184-02-3

Chemical Structure| 227184-02-3

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Product Details of [ 227184-02-3 ]

CAS No. :227184-02-3
Formula : C7H11FO3
M.W : 162.16
SMILES Code : CC(F)C(CC(OCC)=O)=O
MDL No. :MFCD06200831

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Application In Synthesis of [ 227184-02-3 ]

* 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.

  • Downstream synthetic route of [ 227184-02-3 ]

[ 227184-02-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 349-43-9 ]
  • [ 227184-02-3 ]
YieldReaction ConditionsOperation in experiment
93% In tetrahydrofuran; acetic acid methyl ester; Example 4 Synthesis of methyl and ethyl 4-fluoro-3-oxopentanoates To a liquor in which 1.26 g of 63.7percent sodium hydride was suspended in 10 ml of tetrahydrofuran was added dropwise a mixed solution comprising 2.00 g of <strong>[349-43-9]ethyl 2-fluoropropionate</strong> and 1.86 g of methyl acetate over 10 minutes, and the mixture was then heated at 30 to 35° C. for 4 hours. After completion of the reaction, the mixture was cooled to room temperature, neutralized with 1N-hydrochloric acid and the liquids were separated. The organic layer was quantitated by the gas chromatography internal standard method to find out that 1.43 g (yield: 58percent) of methyl 4-fluoro-3-oxopentanoate and 0.95 g (yield: 35percent) of ethyl 4-fluoro-3-oxopentanoate were formed (total yield: 93percent).
87% In tetrahydrofuran; ethyl acetate; Example 3 Synthesis of ethyl 4-fluoro-3-oxopentanoate To a liquor in which 1.28 g of 62.8percent sodium hydride was suspended in 10 ml of tetrahydrofuran was added dropwise a mixed solution comprising 2.00 g of <strong>[349-43-9]ethyl 2-fluoropropionate</strong> and 1.91 g of ethyl acetate over 10 minutes, and the mixture was then heated at 35 to 40° C. for 4 hours. After completion of the reaction, the mixture was cooled to room temperature, neutralized with 1N-hydrochloric acid and the liquids were separated. The organic layer was quantitated by the gas chromatography internal standard method to find out that 2.35 g of ethyl 4-fluoro-3-oxopentanoate was formed (yield: 87percent). This organic layer was concentrated under reduced pressure, and distilled under reduced pressure to obtain 1.73 g of ethyl 4-fluoro-3-oxopentanoate. Boiling point: 38 to 41° C./2 mmHg Mass analysis value: CI-MS m/e=163 (m+1) 1H-NMR (CDCl3) delta (ppm): 1.26 to 1.32 (3H, m), 1.47 to 1.60 (3H, m), 3.63 to 3.64 (1.72H, d), 4.18 to 4.26 (2H, m), 4.86 to 5.12 (1H, m), 5.31 (0.14H, s), 12.02 (0.14H, s)
 

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