HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458120Generated: October 31, 2026
Diethyl Oxalate → 4-Methyl-2-oxo-4-phenylpentanoic acid ethyl ester
https://huagongshe.com/reaction/458120
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | HCID 178448192 | HCID 178448192 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methyl-2-oxo-4-phenylpentanoic acid ethyl ester | HCID 11333779 | 51% |
Reaction Steps
2-Phenyl-2,2-dimethylethylmagnesium bromide (10 mmol, 20 mL of 0.5 M solution in diethyl ether) was added to solution of diethyl oxalate (1.5 g, 10.5 mmol) in anhydrous THF (20 mL) cooled to −78° C. and maintained under argon. After 1 hour, TLC in hexanes-EtOAc (7:1) indicated most of the diethyl oxalate had been consumed. The reaction mixture was quenched with a saturated solution of ammonium chloride and extracted with three 50 mL portions of EtOAc. The combined extracts were dried over anhydrous sodium sulfate and concentrated in vacuo to give a light brown, thick oil which was purified by flash column chromatography over silica gel eluting with 5% EtOAc in hexanes to yield 4-methyl-2-oxo-4-phenylpentanoic acid ethyl ester as a light yellow oil (1.1 g, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07189758B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-8c441db096274e3fb32b99b04e2b8e66 |
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| Source note | uspto-grants-2007_03 |
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