HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266548Generated: October 30, 2026
Sodium hydride → 2-(4-fluorobenzyl)-3-oxopentanoic Acid Methyl Ester
https://huagongshe.com/reaction/2266548
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluorobenzyl bromide | HCID 68021 | — |
| Reactant | Methyl 3-oxovalerate | HCID 121699 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-fluorobenzyl)-3-oxopentanoic Acid Methyl Ester | HCID 68783175 | — |
Reaction Steps
3-Oxopentanoic acid methyl ester (7.5 g) was added to a stirred suspension of sodium hydride (60% in oil, 4.6 g) in N,N-dimethylformamide (20 mL) and tetrahydrofuran (80 mL) at 0° C. and the resulting mixture stirred at 0° C. for 30 minutes. A solution of 1-bromomethyl-4-fluorobenzene (7.0 mL) in tetrahydrofuran was added and the resulting mixture warmed to room temperature and then stirred at this temperature for 17 hours. The mixture was partitioned between ethyl acetate and water and the aqueous phase extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate and the solvent removed under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with a mixture of cyclohexane and ethyl acetate (19:1 by volume) to afford title compound, 1.0 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858640B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-a507e242d645476f96525c741de41f09 |
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| Source note | uspto-grants-2010_12 |
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